dehydroepiandrosterone has been researched along with Dyspareunia in 30 studies
Dehydroepiandrosterone: A major C19 steroid produced by the ADRENAL CORTEX. It is also produced in small quantities in the TESTIS and the OVARY. Dehydroepiandrosterone (DHEA) can be converted to TESTOSTERONE; ANDROSTENEDIONE; ESTRADIOL; and ESTRONE. Most of DHEA is sulfated (DEHYDROEPIANDROSTERONE SULFATE) before secretion.
dehydroepiandrosterone : An androstanoid that is androst-5-ene substituted by a beta-hydroxy group at position 3 and an oxo group at position 17. It is a naturally occurring steroid hormone produced by the adrenal glands.
Dyspareunia: Recurrent genital pain occurring during, before, or after SEXUAL INTERCOURSE in either the male or the female.
Excerpt | Relevance | Reference |
---|---|---|
"Intravaginal dehydroepiandrosterone (DHEA) is a locally metabolised estrogen and androgen precursor, licensed in 2018 in the EU for moderate to severe vulvovaginal atrophy in postmenopausal women." | 9.51 | Intravaginal dehydroepiandrosterone for genitourinary symptoms of the menopause: Is the evidence sufficient? ( Bruce, D; Holloway, D; Kearley-Shiers, K, 2022) |
"The aim of this study is to confirm the local beneficial effects of intravaginal dehydroepiandrosterone (DHEA, Prasterone) on moderate to severe dyspareunia or pain at sexual activity, the most frequent symptom of vulvovaginal atrophy due to menopause or genitourinary syndrome of menopause (GSM)." | 9.27 | Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause. ( Archer, DF; Balser, J; BSc, AB; Côté, I; Frenette, L; Koltun, W; Labrie, F; Lavoie, L; Martel, C; Montesino, M; Moyneur, É; Parent, J; Portman, D; Vachon, A; Vaillancourt, M; Young, D, 2018) |
"The aim of this study is to confirm the local beneficial effects of intravaginal dehydroepiandrosterone (DHEA, Prasterone) on moderate to severe dyspareunia or pain at sexual activity, the most frequent symptom of vulvovaginal atrophy due to menopause or genitourinary syndrome of menopause (GSM)." | 9.22 | Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause. ( Archer, DF; Balser, J; Beauregard, A; Côté, I; Frenette, L; Koltun, W; Labrie, F; Lavoie, L; Martel, C; Montesino, M; Moyneur, É; Parent, J; Portman, D; Vachon, A; Vaillancourt, M; Young, D, 2016) |
"5 mg) dehydroepiandrosterone (DHEA, prasterone) for 12 weeks has shown clinically and statistically significant effects on moderate to severe (MS) dyspareunia as the most bothersome symptom (MBS), the present study analyzes the effect of a reduced dosing regimen on MBS vaginal dryness." | 9.20 | Decreased efficacy of twice-weekly intravaginal dehydroepiandrosterone on vulvovaginal atrophy. ( Archer, DF; Ayotte, N; Balser, J; Bouchard, C; Cooper, TA; Côté, I; Elfassi, É; Grainger, DA; Koltun, W; Labrie, C; Labrie, F; Lavoie, L; Martel, C; Martens, M; Portman, DJ; Waldbaum, AS, 2015) |
"To examine the effect of intravaginal dehydroepiandrosterone (DHEA) on pain at sexual activity (dyspareunia) identified as the most bothersome symptom of vaginal atrophy in postmenopausal women at both screening and day 1." | 9.15 | Intravaginal dehydroepiandrosterone (prasterone), a highly efficient treatment of dyspareunia. ( Archer, DF; Ayotte, N; Balser, J; Baron, M; Berger, L; Bouchard, C; Côté, I; Cusan, L; Dubé, R; Fortier, M; Gilbert, L; Girard, G; Gomez, JL; Labrie, C; Labrie, F; Lavoie, L; Martel, C; Moreau, M, 2011) |
"To compare treatment efficacy and safety parameters a total of 55 premenopausal women with histologically proven endometriosis (stage II-IV) were randomized to receive the LHRH-analogue depot triptorelin (n = 30) or the steroid danazol (n = 25) for a total of 24 weeks." | 9.08 | A randomized, comparative trial of triptorelin depot (D-Trp6-LHRH) and danazol in the treatment of endometriosis. ( Cirkel, U; Ochs, H; Schneider, HP, 1995) |
"The effects of intravaginal administration of dehydroepiandrosterone (DHEA) for the management of symptomatic vulvovaginal atrophy are reviewed." | 8.91 | Dehydroepiandrosterone intra vaginal administration for the management of postmenopausal vulvovaginal atrophy. ( Archer, DF, 2015) |
"Intravaginal dehydroepiandrosterone (DHEA) is a locally metabolised estrogen and androgen precursor, licensed in 2018 in the EU for moderate to severe vulvovaginal atrophy in postmenopausal women." | 5.51 | Intravaginal dehydroepiandrosterone for genitourinary symptoms of the menopause: Is the evidence sufficient? ( Bruce, D; Holloway, D; Kearley-Shiers, K, 2022) |
"The aim of this study is to confirm the local beneficial effects of intravaginal dehydroepiandrosterone (DHEA, Prasterone) on moderate to severe dyspareunia or pain at sexual activity, the most frequent symptom of vulvovaginal atrophy due to menopause or genitourinary syndrome of menopause (GSM)." | 5.27 | Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause. ( Archer, DF; Balser, J; BSc, AB; Côté, I; Frenette, L; Koltun, W; Labrie, F; Lavoie, L; Martel, C; Montesino, M; Moyneur, É; Parent, J; Portman, D; Vachon, A; Vaillancourt, M; Young, D, 2018) |
" Topical interventions (vaginal gels or creams) were able to alleviate vaginal dryness and dyspareunia, with intravaginal dehydroepiandrosterone (DHEA) (6." | 5.22 | Efficacy of interventions to manage sexual dysfunction in women with cancer: a systematic review. ( Febrina, F; Marino, JL; Peate, M; Triyoga, IF; White, M, 2022) |
"The objective of the study is to evaluate the acceptability of the intravaginal administration of ovules/suppositories of DHEA (dehydroepiandrosterone, prasterone) for the treatment of vulvovaginal atrophy (VVA) in women with moderate to severe dyspareunia who were administered daily for 12 weeks intravaginal 0." | 5.22 | Evaluation of the acceptability of intravaginal prasterone ovule administration using an applicator. ( Archer, DF; Balser, J; Beauregard, A; Côté, I; Labrie, F; Lavoie, L; Martel, C; Montesino, M; Moyneur, E; Vaillancourt, M; Zerhouni, J, 2016) |
"The aim of this study is to confirm the local beneficial effects of intravaginal dehydroepiandrosterone (DHEA, Prasterone) on moderate to severe dyspareunia or pain at sexual activity, the most frequent symptom of vulvovaginal atrophy due to menopause or genitourinary syndrome of menopause (GSM)." | 5.22 | Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause. ( Archer, DF; Balser, J; Beauregard, A; Côté, I; Frenette, L; Koltun, W; Labrie, F; Lavoie, L; Martel, C; Montesino, M; Moyneur, É; Parent, J; Portman, D; Vachon, A; Vaillancourt, M; Young, D, 2016) |
"5 mg) dehydroepiandrosterone (DHEA, prasterone) for 12 weeks has shown clinically and statistically significant effects on moderate to severe (MS) dyspareunia as the most bothersome symptom (MBS), the present study analyzes the effect of a reduced dosing regimen on MBS vaginal dryness." | 5.20 | Decreased efficacy of twice-weekly intravaginal dehydroepiandrosterone on vulvovaginal atrophy. ( Archer, DF; Ayotte, N; Balser, J; Bouchard, C; Cooper, TA; Côté, I; Elfassi, É; Grainger, DA; Koltun, W; Labrie, C; Labrie, F; Lavoie, L; Martel, C; Martens, M; Portman, DJ; Waldbaum, AS, 2015) |
"To compare treatment efficacy and safety parameters a total of 55 premenopausal women with histologically proven endometriosis (stage II-IV) were randomized to receive the LHRH-analogue depot triptorelin (n = 30) or the steroid danazol (n = 25) for a total of 24 weeks." | 5.08 | A randomized, comparative trial of triptorelin depot (D-Trp6-LHRH) and danazol in the treatment of endometriosis. ( Cirkel, U; Ochs, H; Schneider, HP, 1995) |
" estradiol, dehydroepiandrosterone [DHEA], progesterone) that causes menopause commonly affects a woman's general health and produces bothersome physical changes that may interfere with normal sexual and genitourinary functioning." | 5.01 | Treatment of moderate to severe dyspareunia with intravaginal prasterone therapy: a review. ( Goldstein, SR; Kagan, R; Portman, DJ, 2019) |
"The effects of intravaginal administration of dehydroepiandrosterone (DHEA) for the management of symptomatic vulvovaginal atrophy are reviewed." | 4.91 | Dehydroepiandrosterone intra vaginal administration for the management of postmenopausal vulvovaginal atrophy. ( Archer, DF, 2015) |
" The use of estrogen agonists/antagonists and intravaginal dehydroepiandrosterone (DHEA) have both been shown to positively affect vaginal atrophy symptoms without inducing endometrial proliferation." | 4.86 | Vulvovaginal atrophy: current and future therapies (CME). ( Ibe, C; Simon, JA, 2010) |
" More recently, double-blind, placebo-controlled clinical trials have demonstrated that local vaginal dehydroepiandrosterone improves symptoms in postmenopausal women, including moderate to severe dyspareunia." | 3.88 | The role of androgens in the treatment of genitourinary syndrome of menopause (GSM): International Society for the Study of Women's Sexual Health (ISSWSH) expert consensus panel review. ( Archer, DF; Bachmann, G; Davis, SR; Goldstein, AT; Goldstein, I; Kellogg-Spadt, S; Kim, NN; Lowenstein, L; Nappi, RE; Pinkerton, JV; Simon, JA; Stuenkel, CA; Traish, AM; Vignozzi, L, 2018) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (6.67) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 24 (80.00) | 24.3611 |
2020's | 4 (13.33) | 2.80 |
Authors | Studies |
---|---|
Febrina, F | 1 |
Triyoga, IF | 1 |
White, M | 1 |
Marino, JL | 1 |
Peate, M | 1 |
Kearley-Shiers, K | 1 |
Holloway, D | 1 |
Bruce, D | 1 |
Cipriani, S | 1 |
Maseroli, E | 1 |
Ravelli, SA | 1 |
Vignozzi, L | 2 |
Gajarawala, SN | 1 |
Wood, TA | 1 |
Stanton, AP | 1 |
Holton, M | 1 |
Thorne, C | 1 |
Goldstein, AT | 2 |
Shifren, JL | 1 |
Simon, JA | 2 |
Goldstein, I | 1 |
Kim, NN | 1 |
Davis, SR | 1 |
Kellogg-Spadt, S | 1 |
Lowenstein, L | 1 |
Pinkerton, JV | 1 |
Stuenkel, CA | 1 |
Traish, AM | 1 |
Archer, DF | 11 |
Bachmann, G | 1 |
Nappi, RE | 1 |
Labrie, F | 10 |
Koltun, W | 6 |
Vachon, A | 3 |
Young, D | 3 |
Frenette, L | 3 |
Portman, D | 3 |
Montesino, M | 5 |
Côté, I | 10 |
Parent, J | 3 |
Lavoie, L | 10 |
BSc, AB | 1 |
Martel, C | 10 |
Vaillancourt, M | 5 |
Balser, J | 10 |
Moyneur, É | 6 |
Portman, DJ | 4 |
Goldstein, SR | 1 |
Kagan, R | 1 |
Hayes, R | 1 |
Birch, M | 1 |
Heo, YA | 1 |
Archer, D | 1 |
Bouchard, C | 5 |
Fortier, M | 2 |
Cusan, L | 4 |
Gomez, JL | 2 |
Girard, G | 3 |
Baron, M | 3 |
Ayotte, N | 4 |
Moreau, M | 2 |
Dubé, R | 2 |
Labrie, C | 5 |
Gilbert, L | 2 |
Elfassi, É | 1 |
Grainger, DA | 1 |
Cooper, TA | 1 |
Martens, M | 1 |
Waldbaum, AS | 2 |
Gallagher, JC | 1 |
Blouin, F | 1 |
Beauregard, A | 5 |
Scheffers, CS | 1 |
Armstrong, S | 1 |
Cantineau, AE | 1 |
Farquhar, C | 1 |
Jordan, V | 1 |
Derogatis, L | 1 |
Zerhouni, J | 1 |
Gandhi, J | 1 |
Chen, A | 1 |
Dagur, G | 1 |
Suh, Y | 1 |
Smith, N | 1 |
Cali, B | 1 |
Khan, SA | 1 |
Aschenbrenner, DS | 1 |
Basson, R | 1 |
Wierman, ME | 1 |
van Lankveld, J | 1 |
Brotto, L | 1 |
Ibe, C | 1 |
Berger, L | 1 |
Dickson, GM | 1 |
Cirkel, U | 1 |
Ochs, H | 1 |
Schneider, HP | 1 |
Kuckatz, C | 1 |
Eicher, W | 1 |
Klinga, K | 1 |
Mueck, AO | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A Randomized, Double-blind, Placebo-controlled Trial on the Preventive Effect of Intravaginal Prasterone (DHEA, Intrarosa®) on Recurrent Urinary Tract Infections in Women With Genitourinary Syndrome of Menopause[NCT03854396] | Phase 3 | 0 participants (Actual) | Interventional | 2020-05-31 | Withdrawn (stopped due to due to termination of ISR by PI with agreement by grant sponsor) | ||
Open-Label Vulvoscopy Photography Study of Changes in Vulva, Vestibule, Urethral Meatus and Vagina 20 Weeks Post Daily Administration of 6.5 Mg Vaginal Prasterone in Menopausal Women With Moderate to Severe Dyspareunia[NCT03568604] | Phase 4 | 18 participants (Actual) | Interventional | 2018-08-07 | Completed | ||
Topical DHEA Against Vaginal Atrophy (3-Month Placebo-Controlled Double-Blind Randomized Phase III Study)[NCT01846442] | Phase 3 | 218 participants (Actual) | Interventional | 2007-06-30 | Completed | ||
[NCT01358760] | Phase 3 | 450 participants (Actual) | Interventional | 2011-06-30 | Completed | ||
A Review on the Clinical Outcome of Chinese Women With Moderate to Severe Symptoms of Genitourinary Syndrome of Menopause (GSM) Treated With Vaginal Dehydroepiandrosterone (DHEA)[NCT05434351] | 4 participants (Actual) | Observational | 2022-08-01 | Terminated (stopped due to inadequate sample and only few patients were prescribed with vaginal DHEA) | |||
Effect of Intravaginal Prasterone (DHEA) on Moderate to Severe Symptoms of Vulvovaginal Atrophy Due to Menopause, in Women Under Treatment With an Aromatase Inhibitor for Breast Cancer - (Placebo-Controlled, Double Blind and Randomized Phase III Study)[NCT03740945] | Phase 3 | 0 participants (Actual) | Interventional | 2018-11-06 | Withdrawn (stopped due to Business decision to not perform this study.) | ||
DHEA Against Vaginal Atrophy (Placebo-controlled, Double-blind and Randomized Phase III Study of 3-month Intravaginal DHEA)[NCT01256684] | Phase 3 | 255 participants (Actual) | Interventional | 2010-12-31 | Completed | ||
A Placebo-controlled Study Examining the Morphological/Biochemical Effects of Intrarosa on the Vulvar Vestibule and Vagina in Women With Genitourinary Syndrome of Menopause/Vulvovaginal Atrophy[NCT03782480] | Phase 3 | 40 participants (Anticipated) | Interventional | 2019-03-02 | Recruiting | ||
DHEA Against Vaginal Atrophy - Safety Study of 12 Months[NCT01256671] | Phase 3 | 530 participants (Actual) | Interventional | 2010-12-31 | Completed | ||
[NCT02013544] | Phase 3 | 558 participants (Actual) | Interventional | 2014-02-28 | Completed | ||
Prasterone (DHEA) for the Treatment of Hypoactive Sexual Desire Disorder (HSDD) - Second Study (Placebo-Controlled, Double-Blind and Randomized Phase III Study of Intravaginal Prasterone)[NCT03619005] | Phase 3 | 0 participants (Actual) | Interventional | 2018-11-13 | Withdrawn (stopped due to Business decision to not continue this study (only few subjects were screened).) | ||
Prasterone (DHEA) for the Treatment of Hypoactive Sexual Desire Disorder (HSDD) - (Placebo-Controlled, Double Blind and Randomized Phase III Study of Intravaginal Prasterone)[NCT03287232] | Phase 3 | 653 participants (Actual) | Interventional | 2017-10-16 | Completed | ||
Compare the Effectiveness and Side Effects of Vaginal Estrogen and Platelet-rich Plasma Over Women With Genitourinary Syndrome of Menopause[NCT05483634] | 40 participants (Anticipated) | Observational | 2022-10-28 | Not yet recruiting | |||
Effectiveness of C02 Microfractionated Laser in Conjunction With Topical Regenerative Therapy in the Management of Vulvo-vaginal Atrophy in Patients With a History of Breast Cancer. Randomized Experimental and Comparative Study.[NCT05585476] | 98 participants (Anticipated) | Interventional | 2022-12-31 | Not yet recruiting | |||
Effects of Vaginal Oxytocin Gel on Vaginal Cytologic Parameters in Postmenopausal Woman: A Randomized Placebo-controlled Trial[NCT05627791] | Phase 2/Phase 3 | 6 participants (Actual) | Interventional | 2022-11-30 | Terminated (stopped due to Unable to recuit participant number in time.) | ||
Photobiomodulation Effect on Vulvovaginal Atrophy in Postmenopausal Women: Randomized and Controlled Trial.[NCT04487392] | Phase 2 | 0 participants (Actual) | Interventional | 2020-12-15 | Withdrawn (stopped due to The student do not start the study) | ||
Effect of Combined Antihypertensive Therapy on Blood Pressure and Sexual Function in Patients With Essential Hypertension[NCT01238705] | Phase 4 | 280 participants (Anticipated) | Interventional | 2008-04-30 | Recruiting | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
To evaluate the aspect of the vaginal mucosa and the local tolerance to DHEA suppository, the vaginal color (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01846442)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline | |
0.25% DHEA | 3.0 | 2.0 | -1.0 |
0.50% DHEA | 3.1 | 1.8 | -1.3 |
1.00% DHEA | 3.1 | 1.6 | -1.5 |
Placebo | 3.1 | 2.7 | -0.5 |
To evaluate the aspect of the vaginal mucosa and the local tolerance to DHEA suppository, the vaginal epithelial integrity (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01846442)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline | |
0.25% DHEA | 2.7 | 1.7 | -1.0 |
0.50% DHEA | 2.8 | 1.5 | -1.3 |
1.00% DHEA | 2.7 | 1.4 | -1.3 |
Placebo | 2.8 | 2.4 | -0.4 |
To evaluate the aspect of the vaginal mucosa and the local tolerance to DHEA suppository, the vaginal epithelial surface thickness(one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01846442)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline | |
0.25% DHEA | 2.9 | 1.9 | -1.0 |
0.50% DHEA | 3.1 | 1.8 | -1.3 |
1.00% DHEA | 3.0 | 1.6 | -1.4 |
Placebo | 3.0 | 2.6 | -0.4 |
To evaluate the aspect of the vaginal mucosa and the local tolerance to DHEA suppository, the vaginal secretions (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy were analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01846442)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline | |
0.25% DHEA | 3.1 | 1.9 | -1.2 |
0.50% DHEA | 3.2 | 1.8 | -1.4 |
1.00% DHEA | 3.0 | 1.5 | -1.4 |
Placebo | 3.1 | 2.7 | -0.4 |
The severity of dyspareunia was evaluated by a questionnaire. The severity of dyspareunia recorded as none, mild, moderate or severe was analyzed using the score values of 0, 1, 2 or 3, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01846442)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline | |
0.25% DHEA | 2.8 | 1.4 | -1.3 |
0.50% DHEA | 2.7 | 1.1 | -1.6 |
1.00% DHEA | 2.6 | 1.2 | -1.4 |
Placebo | 2.8 | 2.3 | -0.4 |
The percentage of parabasal cells was determined from the vaginal smears collected during the study. A 100-cell count was performed by a central laboratory to classify cells as parabasal (P) (including basal), intermediate (I), and superficial (S) squamous cell types. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01846442)
Timeframe: Baseline and Week 12
Intervention | percentage of parabasal cells (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline | |
0.25% DHEA | 65.5 | 16.9 | -48.6 |
0.50% DHEA | 53.4 | 11.0 | -42.4 |
1.00% DHEA | 61.8 | 6.90 | -54.9 |
Placebo | 46.7 | 47.8 | 1.1 |
The percentage of superficial cells was determined from the vaginal smears collected during the study. A 100-cell count was performed by a central laboratory to classify cells as parabasal (P) (including basal), intermediate (I), and superficial (S) squamous cell types. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01846442)
Timeframe: Baseline and Week 12
Intervention | percentage of superficial cells (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline | |
0.25% DHEA | 0.4 | 5.7 | 5.3 |
0.50% DHEA | 0.4 | 5.2 | 4.8 |
1.00% DHEA | 0.4 | 6.5 | 6.1 |
Placebo | 0.6 | 0.5 | -0.1 |
A pH strip was applied directly to the lateral wall of the vagina using forceps. The change in color of the pH indicator strip was compared to the color chart for pH evaluation. The corresponding pH value (with one decimal) was recorded. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01846442)
Timeframe: Baseline and Week 12
Intervention | pH (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline | |
0.25% DHEA | 6.6 | 5.5 | -1.1 |
0.50% DHEA | 6.6 | 5.2 | -1.5 |
1.00% DHEA | 6.5 | 5.1 | -1.4 |
Placebo | 6.5 | 6.0 | -0.5 |
The percentage of parabasal cells was determined from the vaginal smears collected during the study. A 100-cell count was performed by a central laboratory to classify cells as parabasal (P) (including basal), intermediate (I), and superficial (S) squamous cell types. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01358760)
Timeframe: Baseline and Week 12
Intervention | percentage of parabasal cells (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 56.74 | 39.23 | -17.51 |
0.50% DHEA | 59.54 | 33.02 | -26.52 |
Placebo | 60.66 | 62.22 | 1.56 |
The percentage of superficial cells was determined from the vaginal smears collected during the study. A 100-cell count was performed by a central laboratory to classify cells as parabasal (P) (including basal), intermediate (I), and superficial (S) squamous cell types. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01358760)
Timeframe: Baseline and Week 12
Intervention | percentage of superficial cells (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 1.12 | 3.43 | 2.31 |
0.50% DHEA | 0.93 | 3.58 | 2.66 |
Placebo | 0.97 | 1.80 | 0.83 |
The severity of dyspareunia was evaluated by a questionnaire filled out by women. The severity of dyspareunia recorded as none, mild, moderate or severe was analyzed using the score values of 0, 1, 2 or 3, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01358760)
Timeframe: Baseline and Week 12
Intervention | Severity score (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 2.58 | 1.48 | -1.10 |
0.50% DHEA | 2.60 | 1.54 | -1.06 |
Placebo | 2.56 | 1.78 | -0.78 |
The severity of vaginal dryness was evaluated by a questionnaire filled out by women. The severity of dryness recorded as none, mild, moderate or severe was analyzed using the score values of 0, 1, 2 or 3, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01358760)
Timeframe: Baseline and Week 12
Intervention | Severity score (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 2.37 | 1.10 | -1.28 |
0.50% DHEA | 2.35 | 1.13 | -1.22 |
Placebo | 2.38 | 1.27 | -1.12 |
To evaluate the aspect of the mucosa and the local tolerance to prasterone ovules, the vaginal color (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01358760)
Timeframe: Baseline and Week 12
Intervention | Severity score (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 2.60 | 2.16 | -0.45 |
0.50% DHEA | 2.65 | 2.12 | -0.53 |
Placebo | 2.66 | 2.31 | -0.35 |
To evaluate the aspect of the mucosa and the local tolerance to prasterone ovules, the vaginal epithelial integrity (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01358760)
Timeframe: Baseline and Week 12
Intervention | Severity score (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 2.19 | 1.74 | -0.46 |
0.50% DHEA | 2.19 | 1.69 | -0.50 |
Placebo | 2.32 | 1.94 | -0.38 |
To evaluate the aspect of the mucosa and the local tolerance to prasterone ovules, the vaginal epithelial surface thickness (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01358760)
Timeframe: Baseline and Week 12
Intervention | Severity score (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 2.66 | 2.25 | -0.40 |
0.50% DHEA | 2.72 | 2.16 | -0.56 |
Placebo | 2.78 | 2.40 | -0.38 |
To evaluate the aspect of the mucosa and the local tolerance to prasterone ovules, the vaginal secretions (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy were analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01358760)
Timeframe: Baseline and Week 12
Intervention | Severity score (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 2.55 | 2.07 | -0.48 |
0.50% DHEA | 2.55 | 2.07 | -0.48 |
Placebo | 2.71 | 2.33 | -0.38 |
A pH strip fixed on an Ayre spatula (or equivalent) was applied directly to the lateral wall of the vagina. The change in color of the pH indicator strip was compared to the color chart for pH evaluation. The corresponding pH value (with one decimal) was recorded. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01358760)
Timeframe: Baseline and Week 12
Intervention | pH units (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 6.27 | 5.69 | -0.58 |
0.50% DHEA | 6.29 | 5.67 | -0.62 |
Placebo | 6.34 | 6.06 | -0.28 |
The percentage of parabasal cell was determined from the vaginal smears collected during the study. A 100-cell count was performed by a central laboratory to classify cells as parabasal (P) (including the basal), intermediate (I), and superficial (S) squamous cell types. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01256684)
Timeframe: Baseline and Week 12
Intervention | Percentage of parabasal cells (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 65.72 | 28.43 | -37.29 |
0.50% DHEA | 65.05 | 17.65 | -47.40 |
Placebo | 68.48 | 66.86 | -1.62 |
The percentage of superficial cell was determined from the vaginal smears collected during the study. A 100-cell count was performed by a central laboratory to classify cells as parabasal (P) (including the basal), intermediate (I), and superficial (S) squamous cell types. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01256684)
Timeframe: Baseline and Week 12
Intervention | Percentage of superficial cells (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 0.68 | 5.43 | 4.75 |
0.50% DHEA | 0.68 | 6.30 | 5.62 |
Placebo | 0.73 | 1.64 | 0.91 |
The severity of dyspareunia was evaluated by a questionnaire filled out by women. The severity of dyspareunia recorded as none, mild, moderate or severe was analyzed using the score values of 0, 1, 2 or 3, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01256684)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 2.56 | 1.54 | -1.01 |
0.50% DHEA | 2.63 | 1.36 | -1.27 |
Placebo | 2.58 | 1.71 | -0.87 |
To evaluate the aspect of the mucosa and the local tolerance to DHEA suppositories, the vaginal color (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was then analyzed using the values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01256684)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 2.94 | 2.27 | -0.67 |
0.50% DHEA | 2.94 | 2.05 | -0.89 |
Placebo | 2.82 | 2.56 | -0.26 |
To evaluate the aspect of the mucosa and the local tolerance to DHEA suppositories, the vaginal epithelial integrity (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was then analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01256684)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 2.57 | 1.92 | -0.65 |
0.50% DHEA | 2.57 | 1.69 | -0.88 |
Placebo | 2.58 | 2.13 | -0.45 |
To evaluate the aspect of the mucosa and the local tolerance to DHEA suppositories, the vaginal epithelial surface thickness (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was then analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01256684)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 2.90 | 2.32 | -0.58 |
0.50% DHEA | 2.89 | 2.14 | -0.75 |
Placebo | 2.91 | 2.57 | -0.34 |
To evaluate the aspect of the mucosa and the local tolerance to DHEA suppositories, the vaginal secretions (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy were then analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01256684)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 2.81 | 2.10 | -0.71 |
0.50% DHEA | 2.83 | 1.95 | -0.88 |
Placebo | 2.78 | 2.36 | -0.42 |
The severity of vaginal dryness was evaluated by a questionnaire filled out by women. The severity of vaginal dryness recorded as none, mild, moderate or severe was analyzed using the score values of 0, 1, 2 or 3, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01256684)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 2.20 | 0.91 | -1.29 |
0.50% DHEA | 2.37 | 0.92 | -1.45 |
Placebo | 2.33 | 1.32 | -1.02 |
A pH strip fixed on an Ayre spatula (or equivalent) was applied directly to the lateral wall of the vagina. The change in color of the pH indicator strip was compared to the color chart for pH evaluation. The corresponding pH value (with one decimal) was recorded. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT01256684)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.25% DHEA | 6.48 | 5.70 | -0.77 |
0.50% DHEA | 6.47 | 5.43 | -1.04 |
Placebo | 6.51 | 6.31 | -0.21 |
The severity of dyspareunia was evaluated by a questionnaire. The severity of dyspareunia recorded as none, mild, moderate or severe was analyzed using the score values of 0, 1, 2 or 3, respectively. Data obtained at Baseline and Week 52 as well as the change from Baseline to Week 52 are presented. (NCT01256671)
Timeframe: Baseline and Week 52
Intervention | units on a scale (Mean) | |||||
---|---|---|---|---|---|---|
Baseline: Subgroup MS | Week 52: Subgroup MS | Change from Baseline: Subgroup MS | Baseline: Subgroup MBS/MS | Week 52: Subgroup MBS/MS | Change from Baseline: Subgroup MBS/MS | |
0.50% DHEA | 2.53 | 0.85 | -1.68 | 2.57 | 0.87 | -1.69 |
The severity of irritation/itching was evaluated by a questionnaire. The severity of irritation/itching recorded as none, mild, moderate or severe was analyzed using the score values of 0, 1, 2 or 3, respectively. Data obtained at Baseline and Week 52 as well as the change from Baseline to Week 52 are presented. (NCT01256671)
Timeframe: Baseline and Week 52
Intervention | units on a scale (Mean) | |||||
---|---|---|---|---|---|---|
Baseline: Subgroup MS | Week 52: Subgroup MS | Change from Baseline: Subgroup MS | Baseline: Subgroup MBS/MS | Week 52: Subgroup MBS/MS | Change from Baseline: Subgroup MBS/MS | |
0.50% DHEA | 2.10 | 0.60 | -1.50 | 2.13 | 0.74 | -1.39 |
The severity of vaginal dryness was evaluated by a questionnaire. The severity of vaginal dryness recorded as none, mild, moderate or severe was analyzed using the score values of 0, 1, 2 or 3, respectively. Data obtained at Baseline and Week 52 as well as the change from Baseline to Week 52 are presented. (NCT01256671)
Timeframe: Baseline and Week 52
Intervention | units on a scale (Mean) | |||||
---|---|---|---|---|---|---|
Baseline: Subgroup MS | Week 52: Subgroup MS | Change from Baseline: Subgroup MS | Baseline: Subgroup MBS/MS | Week 52: Subgroup MBS/MS | Change from Baseline: Subgroup MBS/MS | |
0.50% DHEA | 2.22 | 0.59 | -1.63 | 2.19 | 0.67 | -1.52 |
The percentage of parabasal cells was determined from the vaginal smears collected during the study. A 100-cell count was performed by a central laboratory to classify cells as parabasal (P) (including basal), intermediate (I), and superficial (S) squamous cell types. Data obtained at Baseline and Week 52 as well as the change from Baseline to Week 52 are presented. (NCT01256671)
Timeframe: Baseline and Week 52
Intervention | percentage of parabasal cells (Mean) | |||||
---|---|---|---|---|---|---|
Baseline: Subgroup ALL | Week 52: Subgroup ALL | Change from Baseline: Subgroup ALL | Baseline: Subgroup VVA | Week 52: Subgroup VVA | Change from Baseline: Subgroup VVA | |
0.50% DHEA | 55.49 | 12.81 | -42.67 | 63.95 | 14.80 | -49.14 |
The percentage of superficial cells was determined from the vaginal smears collected during the study. A 100-cell count was performed by a central laboratory to classify cells as parabasal (P) (including basal), intermediate (I), and superficial (S) squamous cell types. Data obtained at Baseline and Week 52 as well as the change from Baseline to Week 52 are presented. (NCT01256671)
Timeframe: Baseline and Week 52
Intervention | percentage of superficial cells (Mean) | |||||
---|---|---|---|---|---|---|
Baseline: Subgroup ALL | Week 52: Subgroup ALL | Change from Baseline: Subgroup ALL | Baseline: Subgroup VVA | Week 52: Subgroup VVA | Change from Baseline: Subgroup VVA | |
0.50% DHEA | 2.02 | 9.42 | 7.41 | 0.96 | 8.81 | 7.85 |
A pH strip fixed on an Ayre spatula (or equivalent) was applied directly to the lateral wall of the vagina. The change in color of the pH indicator strip was compared to the color chart for pH evaluation. The corresponding pH value (with one decimal) was recorded. Data obtained at Baseline and Week 52 as well as the change from Baseline to Week 52 are presented. (NCT01256671)
Timeframe: Baseline and Week 52
Intervention | pH (Mean) | |||||
---|---|---|---|---|---|---|
Baseline: Subgroup ALL | Week 52: Subgroup ALL | Change from Baseline: Subgroup ALL | Baseline: Subgroup VVA | Week 52: Subgroup VVA | Change from Baseline: Subgroup VVA | |
0.50% DHEA | 6.23 | 5.09 | -1.14 | 6.40 | 5.13 | -1.27 |
The long-term safety of intravaginal prasterone has been evaluated on different parameters including the endometrium. For this purpose, endometrial biopsies were performed at screening and at the end of the study (52 weeks) or at discontinuation visit for women who were exposed to intravaginal DHEA (prasterone) for at least 12 weeks. At screening, the endometrium had to be atrophic/inactive for women to be enrolled in the study. Only the end-of-study data are presented. (NCT01256671)
Timeframe: Baseline and Week 52 (or discontinuation)
Intervention | Participants (Count of Participants) | |
---|---|---|
Endometrium: Atrophic/Inactive | Endometrium: No/Insufficient Tissue for Diagnosis | |
0.50% DHEA | 421 | 36 |
The long-term safety of intravaginal prasterone has been evaluated on different parameters including the serum levels of DHEA and its metabolites. For this purpose, blood samples were collected at Baseline and different post-Baseline timepoints for the determination of serum steroid levels by a central laboratory using validated liquid chromatography tandem mass spectrometry (LC-MS/MS) methods. The serum levels of dehydroepiandrosterone (DHEA), estradiol (E2) and testosterone (TESTO) obtained at Baseline and Week 52 as well as the change from Baseline to Week 52 are presented. (NCT01256671)
Timeframe: Baseline and Week 52
Intervention | pg/mL (Mean) | ||||||||
---|---|---|---|---|---|---|---|---|---|
DHEA: Baseline | DHEA: Week 52 | DHEA: Change from Baseline | E2: Baseline | E2: Week 52 | E2: Change from Baseline | TESTO: Baseline | TESTO: Week 52 | TESTO: Change from Baseline | |
0.50% DHEA | 2071.61 | 2997.25 | 925.65 | 6.05 | 4.46 | -1.59 | 161.28 | 189.44 | 28.17 |
The percentage of parabasal cells was determined from the vaginal smears collected during the study. A 100-cell count was performed by a central laboratory to classify cells as parabasal (P) (including basal), intermediate (I), and superficial (S) squamous cell types. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT02013544)
Timeframe: Baseline and Week 12
Intervention | Percentage of parabasal cells (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.50% Prasterone (DHEA) | 54.25 | 12.74 | -41.51 |
Placebo | 51.66 | 39.68 | -11.98 |
The percentage of superficial cells was determined from the vaginal smears collected during the study. A 100-cell count was performed by a central laboratory to classify cells as parabasal (P) (including basal), intermediate (I), and superficial (S) squamous cell types. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT02013544)
Timeframe: Baseline and Week 12
Intervention | Percentage of superficial cells (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.50% Prasterone (DHEA) | 1.02 | 11.22 | 10.20 |
Placebo | 1.04 | 2.78 | 1.75 |
The severity of dyspareunia was evaluated by a questionnaire filled out by women. The severity of dyspareunia recorded as none, mild, moderate or severe was analyzed using the score values of 0, 1, 2 or 3, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT02013544)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.50% Prasterone (DHEA) | 2.54 | 1.13 | -1.42 |
Placebo | 2.56 | 1.50 | -1.06 |
To evaluate the aspect of the mucosa and the local tolerance to prasterone ovules, the vaginal color (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT02013544)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.50% Prasterone (DHEA) | 2.75 | 2.03 | -0.73 |
Placebo | 2.67 | 2.34 | -0.33 |
To evaluate the aspect of the mucosa and the local tolerance to prasterone ovules, the vaginal epithelial integrity (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT02013544)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.50% Prasterone (DHEA) | 2.45 | 1.75 | -0.69 |
Placebo | 2.43 | 2.06 | -0.37 |
To evaluate the aspect of the mucosa and the local tolerance to prasterone ovules, the vaginal epithelial surface thickness (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy was analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT02013544)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.50% Prasterone (DHEA) | 2.83 | 2.09 | -0.74 |
Placebo | 2.76 | 2.41 | -0.36 |
To evaluate the aspect of the mucosa and the local tolerance to prasterone ovules, the vaginal secretions (one of the four main signs of vaginal atrophy) evaluated by the physician/gynecologist as corresponding to none, mild, moderate, or severe atrophy were analyzed using the score values of 1, 2, 3 and 4, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT02013544)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.50% Prasterone (DHEA) | 2.70 | 1.97 | -0.73 |
Placebo | 2.63 | 2.24 | -0.39 |
The severity of vaginal dryness was evaluated by a questionnaire filled out by women. The severity of vaginal dryness recorded as none, mild, moderate or severe was analyzed using the score values of 0, 1, 2 or 3, respectively. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT02013544)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.50% Prasterone (DHEA) | 2.30 | 0.86 | -1.44 |
Placebo | 2.30 | 1.13 | -1.17 |
A pH strip fixed on an Ayre spatula (or equivalent) was applied directly to the lateral wall of the vagina. The change in color of the pH indicator strip was compared to the color chart for pH evaluation. The corresponding pH value (with one decimal) was recorded. Data obtained at Baseline and Week 12 as well as the change from Baseline to Week 12 are presented. (NCT02013544)
Timeframe: Baseline and Week 12
Intervention | units on a scale (Mean) | ||
---|---|---|---|
Baseline | Week 12 | Change from Baseline to Week 12 | |
0.50% Prasterone (DHEA) | 6.34 | 5.39 | -0.94 |
Placebo | 6.32 | 6.05 | -0.27 |
10 reviews available for dehydroepiandrosterone and Dyspareunia
Article | Year |
---|---|
Efficacy of interventions to manage sexual dysfunction in women with cancer: a systematic review.
Topics: Cancer Survivors; Dehydroepiandrosterone; Dyspareunia; Female; Humans; Male; Neoplasms; Randomized C | 2022 |
The vagina as source and target of androgens: implications for treatment of GSM/VVA, including DHEA.
Topics: Administration, Intravaginal; Androgens; Atrophy; Dehydroepiandrosterone; Dyspareunia; Estrogens; Fe | 2023 |
An overview of dehydroepiandrosterone (EM-760) as a treatment option for genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Androgens; Atrophy; Dehydroepiandrosterone; Dyspareunia; Estrogens; Fe | 2020 |
Genitourinary Syndrome of Menopause.
Topics: Administration, Intravaginal; Administration, Oral; Atrophy; Dehydroepiandrosterone; Dyspareunia; Es | 2018 |
Treatment of moderate to severe dyspareunia with intravaginal prasterone therapy: a review.
Topics: Administration, Intravaginal; Atrophy; Dehydroepiandrosterone; Dyspareunia; Female; Humans; Menopaus | 2019 |
Prasterone (Intrarosa) for Dyspareunia.
Topics: Adjuvants, Immunologic; Administration, Intravaginal; Dehydroepiandrosterone; Dyspareunia; Female; H | 2019 |
Dehydroepiandrosterone intra vaginal administration for the management of postmenopausal vulvovaginal atrophy.
Topics: Atrophy; Dehydroepiandrosterone; Dyspareunia; Female; Humans; Hydrogen-Ion Concentration; Libido; Ov | 2015 |
Dehydroepiandrosterone for women in the peri- or postmenopausal phase.
Topics: Acne Vulgaris; Dehydroepiandrosterone; Dyspareunia; Estrogens; Female; Hot Flashes; Humans; Perimeno | 2015 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Genitourinary syndrome of menopause: an overview of clinical manifestations, pathophysiology, etiology, evaluation, and management.
Topics: Atrophic Vaginitis; Dehydroepiandrosterone; Dyspareunia; Estrogen Replacement Therapy; Female; Human | 2016 |
Vulvovaginal atrophy: current and future therapies (CME).
Topics: Adjuvants, Immunologic; Aged; Atrophy; Dehydroepiandrosterone; Drug Administration Schedule; Drug Th | 2010 |
13 trials available for dehydroepiandrosterone and Dyspareunia
Article | Year |
---|---|
Intravaginal dehydroepiandrosterone for genitourinary symptoms of the menopause: Is the evidence sufficient?
Topics: Administration, Intravaginal; Atrophy; Dehydroepiandrosterone; Dyspareunia; Female; Humans; Menopaus | 2022 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Adjuvants, Immunologic; Administration, Intravaginal; Adult; Aged; Aged, 80 and over; Atrophy; Dehyd | 2018 |
Lack of influence of dyspareunia on the beneficial effect of intravaginal prasterone (dehydroepiandrosterone, DHEA) on sexual dysfunction in postmenopausal women.
Topics: Administration, Intravaginal; Adult; Aged; Androgens; Arousal; Dehydroepiandrosterone; Double-Blind | 2014 |
Lack of influence of dyspareunia on the beneficial effect of intravaginal prasterone (dehydroepiandrosterone, DHEA) on sexual dysfunction in postmenopausal women.
Topics: Administration, Intravaginal; Adult; Aged; Androgens; Arousal; Dehydroepiandrosterone; Double-Blind | 2014 |
Lack of influence of dyspareunia on the beneficial effect of intravaginal prasterone (dehydroepiandrosterone, DHEA) on sexual dysfunction in postmenopausal women.
Topics: Administration, Intravaginal; Adult; Aged; Androgens; Arousal; Dehydroepiandrosterone; Double-Blind | 2014 |
Lack of influence of dyspareunia on the beneficial effect of intravaginal prasterone (dehydroepiandrosterone, DHEA) on sexual dysfunction in postmenopausal women.
Topics: Administration, Intravaginal; Adult; Aged; Androgens; Arousal; Dehydroepiandrosterone; Double-Blind | 2014 |
Decreased efficacy of twice-weekly intravaginal dehydroepiandrosterone on vulvovaginal atrophy.
Topics: Adjuvants, Immunologic; Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Treatment of pain at sexual activity (dyspareunia) with intravaginal dehydroepiandrosterone (prasterone).
Topics: Administration, Intravaginal; Adult; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; | 2015 |
Prasterone has parallel beneficial effects on the main symptoms of vulvovaginal atrophy: 52-week open-label study.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Prasterone has parallel beneficial effects on the main symptoms of vulvovaginal atrophy: 52-week open-label study.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Prasterone has parallel beneficial effects on the main symptoms of vulvovaginal atrophy: 52-week open-label study.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Prasterone has parallel beneficial effects on the main symptoms of vulvovaginal atrophy: 52-week open-label study.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Influence of treatment of vulvovaginal atrophy with intravaginal prasterone on the male partner.
Topics: Adjuvants, Immunologic; Administration, Intravaginal; Adult; Aged; Aged, 80 and over; Atrophy; Coitu | 2015 |
Influence of treatment of vulvovaginal atrophy with intravaginal prasterone on the male partner.
Topics: Adjuvants, Immunologic; Administration, Intravaginal; Adult; Aged; Aged, 80 and over; Atrophy; Coitu | 2015 |
Influence of treatment of vulvovaginal atrophy with intravaginal prasterone on the male partner.
Topics: Adjuvants, Immunologic; Administration, Intravaginal; Adult; Aged; Aged, 80 and over; Atrophy; Coitu | 2015 |
Influence of treatment of vulvovaginal atrophy with intravaginal prasterone on the male partner.
Topics: Adjuvants, Immunologic; Administration, Intravaginal; Adult; Aged; Aged, 80 and over; Atrophy; Coitu | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Effect of Intravaginal Prasterone on Sexual Dysfunction in Postmenopausal Women with Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Adult; Aged; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dys | 2015 |
Evaluation of the acceptability of intravaginal prasterone ovule administration using an applicator.
Topics: Administration, Intravaginal; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Fem | 2016 |
Evaluation of the acceptability of intravaginal prasterone ovule administration using an applicator.
Topics: Administration, Intravaginal; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Fem | 2016 |
Evaluation of the acceptability of intravaginal prasterone ovule administration using an applicator.
Topics: Administration, Intravaginal; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Fem | 2016 |
Evaluation of the acceptability of intravaginal prasterone ovule administration using an applicator.
Topics: Administration, Intravaginal; Atrophy; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Fem | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Efficacy of intravaginal dehydroepiandrosterone (DHEA) on moderate to severe dyspareunia and vaginal dryness, symptoms of vulvovaginal atrophy, and of the genitourinary syndrome of menopause.
Topics: Administration, Intravaginal; Aged; Dehydroepiandrosterone; Double-Blind Method; Dyspareunia; Female | 2016 |
Intravaginal dehydroepiandrosterone (prasterone), a highly efficient treatment of dyspareunia.
Topics: Administration, Intravaginal; Dehydroepiandrosterone; Dose-Response Relationship, Drug; Double-Blind | 2011 |
Intravaginal dehydroepiandrosterone (prasterone), a highly efficient treatment of dyspareunia.
Topics: Administration, Intravaginal; Dehydroepiandrosterone; Dose-Response Relationship, Drug; Double-Blind | 2011 |
Intravaginal dehydroepiandrosterone (prasterone), a highly efficient treatment of dyspareunia.
Topics: Administration, Intravaginal; Dehydroepiandrosterone; Dose-Response Relationship, Drug; Double-Blind | 2011 |
Intravaginal dehydroepiandrosterone (prasterone), a highly efficient treatment of dyspareunia.
Topics: Administration, Intravaginal; Dehydroepiandrosterone; Dose-Response Relationship, Drug; Double-Blind | 2011 |
A randomized, comparative trial of triptorelin depot (D-Trp6-LHRH) and danazol in the treatment of endometriosis.
Topics: Adult; Danazol; Dehydroepiandrosterone; Dehydroepiandrosterone Sulfate; Delayed-Action Preparations; | 1995 |
[The effects of hormone replacement therapy on ovarian function in premenopausal women after hysterectomy].
Topics: Adult; Dehydroepiandrosterone; Dyspareunia; Estradiol; Estrogen Replacement Therapy; Female; Follicl | 1999 |
7 other studies available for dehydroepiandrosterone and Dyspareunia
Article | Year |
---|---|
What is the role of dehydroepiandrosterone in gynecologic practice?
Topics: Administration, Intravaginal; Administration, Oral; Atrophy; Dehydroepiandrosterone; Dyspareunia; Fe | 2019 |
Prasterone (Intrarosa) for dyspareunia.
Topics: Administration, Intravaginal; Dehydroepiandrosterone; Dyspareunia; Female; Humans; Postmenopause; Tr | 2017 |
The role of androgens in the treatment of genitourinary syndrome of menopause (GSM): International Society for the Study of Women's Sexual Health (ISSWSH) expert consensus panel review.
Topics: Administration, Intravaginal; Aged; Androgens; Atrophy; Consensus; Dehydroepiandrosterone; Dyspareun | 2018 |
Prasterone: A Review in Vulvovaginal Atrophy.
Topics: Administration, Intravaginal; Atrophy; Clinical Trials, Phase III as Topic; Dehydroepiandrosterone; | 2019 |
New Drug Treats Painful Sexual Intercourse in Postmenopausal Women.
Topics: Administration, Intravaginal; Dehydroepiandrosterone; Drug Approval; Dyspareunia; Female; Humans; Po | 2017 |
Summary of the recommendations on sexual dysfunctions in women.
Topics: Adjuvants, Immunologic; Dehydroepiandrosterone; Diagnostic and Statistical Manual of Mental Disorder | 2010 |
Menopause management: how you can do better.
Topics: Acupuncture Therapy; Adjuvants, Immunologic; Administration, Cutaneous; Administration, Topical; Aff | 2012 |