norethindrone acetate has been researched along with Bleeding Between Periods in 7 studies
norethisterone acetate : A 3-oxo Delta(4)-steroid that is norethisterone in which the hydroxy group has been converted to its acetate ester.
Excerpt | Relevance | Reference |
---|---|---|
"To evaluate the efficacy and tolerability of norethindrone acetate (NA) as single-agent hormonal therapy for suppression of endometriosis symptoms in adolescents and young adults." | 7.78 | Use of norethindrone acetate alone for postoperative suppression of endometriosis symptoms. ( Berry, KF; Kaser, DJ; Laufer, MR; Missmer, SA, 2012) |
" The ultra-low dose of ethinyl estradiol did not impact scheduled bleeding or intensity of bleeding, but we observed a slight decline in amenorrhea and slight increase in unscheduled bleeding in obese women compared with other BMI categories." | 5.22 | Body mass index does not affect the efficacy or bleeding profile during use of an ultra-low-dose combined oral contraceptive. ( Archer, DF; Nakajima, ST; Pappadakis, J, 2016) |
"This patient preference prospective study was designed to compare patients' satisfaction in women with endometriosis treated either by an extended-cycle oral contraception (OC) or by norethindrone acetate (NETA)." | 3.88 | Norethindrone acetate versus extended-cycle oral contraceptive (Seasonique ( Barra, F; Ferrero, S; Leone Roberti Maggiore, U; Scala, C; Venturini, PL, 2018) |
"To evaluate the efficacy and tolerability of norethindrone acetate (NA) as single-agent hormonal therapy for suppression of endometriosis symptoms in adolescents and young adults." | 3.78 | Use of norethindrone acetate alone for postoperative suppression of endometriosis symptoms. ( Berry, KF; Kaser, DJ; Laufer, MR; Missmer, SA, 2012) |
"New low-dose formulations of combination oral contraceptives (COCs) are safe and effective, but they may be associated with an increased risk of breakthrough bleeding." | 2.73 | Efficacy and safety of a new 24-day oral contraceptive regimen of norethindrone acetate 1 mg/ethinyl estradiol 20 micro g (Loestrin 24 Fe). ( Archer, DF; Ellman, H; Nakajima, ST, 2007) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (28.57) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (28.57) | 29.6817 |
2010's | 3 (42.86) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Scala, C | 1 |
Leone Roberti Maggiore, U | 1 |
Barra, F | 1 |
Venturini, PL | 1 |
Ferrero, S | 1 |
Nakajima, ST | 2 |
Pappadakis, J | 1 |
Archer, DF | 2 |
Kaser, DJ | 1 |
Missmer, SA | 1 |
Berry, KF | 1 |
Laufer, MR | 1 |
Ellman, H | 1 |
Hammar, ML | 1 |
van de Weijer, P | 1 |
Franke, HR | 1 |
Pornel, B | 1 |
von Mauw, EM | 1 |
Nijland, EA | 1 |
Tokin, R | 1 |
Dimov, I | 1 |
Dzhebarov, S | 1 |
Morini, A | 1 |
Mossa, B | 1 |
Roscetti, C | 1 |
Florio, V | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Open-Label Study of the Safety and Efficacy of a Low Dose Oral Contraceptive Containing Norethindrone Acetate and Ethinyl Estradiol[NCT00391807] | Phase 3 | 1,683 participants (Actual) | Interventional | 2006-11-30 | Completed | ||
A Multicenter, Randomized, Double-Blind, Double Dummy, Group-Comparative Trial to Compare the Effects of Livial® and Activelle ® on the Vaginal Bleeding Pattern, Vasomotor Complaints, Vaginal Atrophy, QoL and Sexual Function[NCT00431093] | Phase 4 | 570 participants (Actual) | Interventional | 2002-11-30 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
(NCT00391807)
Timeframe: 12 cycles, 28 days each (336 days)
Intervention | Days (Median) |
---|---|
Norethindrone/Ethinyl Estradiol | 3.85 |
(NCT00391807)
Timeframe: 2 cycles, 28 days each (56 days)
Intervention | Days (Median) |
---|---|
Norethindrone/Ethinyl Estradiol | 3.93 |
(NCT00391807)
Timeframe: 6 cycles, 28 days each (168 days)
Intervention | Days (Median) |
---|---|
Norethindrone/Ethinyl Estradiol | 3.99 |
MITT Population (NCT00391807)
Timeframe: 13 cycles, 28 days each (1 year)
Intervention | Bleeding/Spotting Days (Mean) |
---|---|
Norethindrone/Ethinyl Estradiol | 1.81 |
MITT Population (NCT00391807)
Timeframe: 2 Cycles, 28 days each (56 days)
Intervention | Bleeding/Spotting Days (Mean) |
---|---|
Norethindrone/Ethinyl Estradiol | 3.21 |
MITT Population (NCT00391807)
Timeframe: 6 cycles, 28 days each (168 days)
Intervention | Bleeding/Spotting Days (Mean) |
---|---|
Norethindrone/Ethinyl Estradiol | 2.00 |
(NCT00391807)
Timeframe: 13 cycles, 28 days each (1 year)
Intervention | Percentage of Participants (Number) |
---|---|
Norethindrone/Ethinyl Estradiol | 49.1 |
(NCT00391807)
Timeframe: 2 cycles, 28 days each (56 days)
Intervention | Percentage of Participants (Number) |
---|---|
Norethindrone/Ethinyl Estradiol | 30.7 |
(NCT00391807)
Timeframe: 6 cycles, 28 days each (168 days)
Intervention | Percentage of Participants (Number) |
---|---|
Norethindrone/Ethinyl Estradiol | 42.9 |
(NCT00391807)
Timeframe: 13 cycles, 28 days each (1 year)
Intervention | Percentage of Participants (Number) |
---|---|
Norethindrone/Ethinyl Estradiol | 22.4 |
(NCT00391807)
Timeframe: 2 cycles, 28 days each (56 days)
Intervention | Percentage of Participants (Number) |
---|---|
Norethindrone/Ethinyl Estradiol | 34.8 |
(NCT00391807)
Timeframe: 6 cycles, 28 days each (168 days)
Intervention | Percentage of Participants (Number) |
---|---|
Norethindrone/Ethinyl Estradiol | 25.0 |
(NCT00391807)
Timeframe: 13 cycles, 28 days each (1 year)
Intervention | Pregnancy Rate (Number) |
---|---|
Norethindrone/Ethinyl Estradiol | 2.554 |
(NCT00391807)
Timeframe: 13 Cycles, 28 days each (1 year)
Intervention | Pregnancy Rate (Number) |
---|---|
Norethindrone/Ethinyl Estradiol | 2.167 |
(NCT00391807)
Timeframe: 13 cycles, 28 days each (1 year)
Intervention | Days (Mean) |
---|---|
Norethindrone/Ethinyl Estradiol | 3.36 |
(NCT00391807)
Timeframe: 2 cycles, 28 days each (56 days)
Intervention | Days (Mean) |
---|---|
Norethindrone/Ethinyl Estradiol | 4.57 |
(NCT00391807)
Timeframe: 6 cycles, 28 days each (168 days)
Intervention | Days (Mean) |
---|---|
Norethindrone/Ethinyl Estradiol | 3.00 |
4 trials available for norethindrone acetate and Bleeding Between Periods
Article | Year |
---|---|
Body mass index does not affect the efficacy or bleeding profile during use of an ultra-low-dose combined oral contraceptive.
Topics: Adolescent; Adult; Amenorrhea; Body Mass Index; Contraceptives, Oral, Combined; Contraceptives, Oral | 2016 |
Efficacy and safety of a new 24-day oral contraceptive regimen of norethindrone acetate 1 mg/ethinyl estradiol 20 micro g (Loestrin 24 Fe).
Topics: Adolescent; Adult; Contraceptives, Oral, Combined; Contraceptives, Oral, Synthetic; Dose-Response Re | 2007 |
Tibolone and low-dose continuous combined hormone treatment: vaginal bleeding pattern, efficacy and tolerability.
Topics: Aged; Contraceptives, Oral, Synthetic; Double-Blind Method; Drug Therapy, Combination; Estradiol; Es | 2007 |
[Emergency ambulatory treatment of dysfunctional metrorrhagia in adolescents].
Topics: Adolescent; Ambulatory Care; Drug Combinations; Drug Evaluation; Emergencies; Ethinyl Estradiol; Fem | 1989 |
3 other studies available for norethindrone acetate and Bleeding Between Periods
Article | Year |
---|---|
Norethindrone acetate versus extended-cycle oral contraceptive (Seasonique
Topics: Adult; Contraceptives, Oral, Synthetic; Drug Combinations; Endometriosis; Ethinyl Estradiol; Female; | 2018 |
Use of norethindrone acetate alone for postoperative suppression of endometriosis symptoms.
Topics: Adolescent; Adult; Contraceptives, Oral, Synthetic; Endometriosis; Female; Humans; Metrorrhagia; Nor | 2012 |
[Therapeutic potentials of treating uterine hemorrhages with norethisterone acetate].
Topics: Adolescent; Adult; Drug Evaluation; Female; Humans; Metrorrhagia; Middle Aged; Norethindrone; Noreth | 1983 |