oxybutynin has been researched along with Depression in 12 studies
oxybutynin: RN given refers to parent cpd
oxybutynin : A racemate comprising equimolar amounts of (R)-oxybutynin and esoxybutynin. An antispasmodic used for the treatment of overactive bladder.
Depression: Depressive states usually of moderate intensity in contrast with MAJOR DEPRESSIVE DISORDER present in neurotic and psychotic disorders.
Excerpt | Relevance | Reference |
---|---|---|
"Six-months analysis of non-interventionally collected observation data of effectiveness of long-term treatment with low-dose 7-day buprenorphine transdermal patch in elderly patients with chronic pain." | 7.79 | [Long-term treatment of chronic pain with low-dose 7-day buprenorphine transdermal patch. Observational data from elderly patients of pain relief and quality of life]. ( Müller-Schwefe, GH; Uberall, MA, 2013) |
"Six-months analysis of non-interventionally collected observation data of effectiveness of long-term treatment with low-dose 7-day buprenorphine transdermal patch in elderly patients with chronic pain." | 3.79 | [Long-term treatment of chronic pain with low-dose 7-day buprenorphine transdermal patch. Observational data from elderly patients of pain relief and quality of life]. ( Müller-Schwefe, GH; Uberall, MA, 2013) |
"A retrospective analysis of patients with OAB who initiated treatment with tolterodine extended release (ER), oxybutynin ER, or oxybutynin immediate release (IR) between January 2001 and December 2002 was conducted to evaluate the frequency, relative risk, resource utilization, and costs related to three specific comorbidities associated with OAB: urinary tract infections (UTIs), depression, and fracture." | 3.73 | Retrospective evaluation of outcomes in patients with overactive bladder receiving tolterodine versus oxybutynin. ( Girase, P; Jumadilova, Z; Ollendorf, DA; Varadharajan, S, 2006) |
"Aim of the study was to reduce the dose and dosing frequency of duloxetine HCl (DXT) by complexation with sulfobutylether-β-cyclodextrin (SBEβCD), an anionic cyclodextrin through permeation enhancement for more effective management of depression." | 1.62 | Transdermal delivery of duloxetine-sulfobutylether-β-cyclodextrin complex for effective management of depression. ( Dahiya, L; Kumar, R; Sarwal, A; Sinha, VR, 2021) |
"Incidences of overactive bladder (OAB) and cognitive dysfunction increase with aging." | 1.42 | Influence of antimuscarinic therapy on cognitive functions and quality of life in geriatric patients treated for overactive bladder. ( Ariogul, S; Cankurtaran, E; Cankurtaran, M; Ergen, A; Esin, E; Halil, M; Kuyumcu, ME; Ozcan, M; Ulger, Z; Yavuz, BB; Yeşil, Y, 2015) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (8.33) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (16.67) | 29.6817 |
2010's | 7 (58.33) | 24.3611 |
2020's | 2 (16.67) | 2.80 |
Authors | Studies |
---|---|
Akkoç, Y | 1 |
Bardak, AN | 1 |
Yıldız, N | 1 |
Özlü, A | 1 |
Erhan, B | 1 |
Yürü, B | 1 |
Öztekin, SNS | 1 |
Türkoğlu, MB | 1 |
Paker, N | 1 |
Yumuşakhuylu, Y | 1 |
Canbaz Kabay, S | 1 |
Ekmekçi, Ö | 1 |
Elbi, H | 1 |
Yüceyar, AN | 1 |
Esin, E | 1 |
Ergen, A | 1 |
Cankurtaran, M | 1 |
Yavuz, BB | 1 |
Halil, M | 1 |
Ulger, Z | 1 |
Yeşil, Y | 1 |
Kuyumcu, ME | 1 |
Ozcan, M | 1 |
Cankurtaran, E | 1 |
Ariogul, S | 1 |
Jumadilova, Z | 1 |
Varadharajan, S | 1 |
Girase, P | 1 |
Ollendorf, DA | 1 |
Lefrandt, JD | 1 |
Maurer, JM | 1 |
Renshaw, DC | 1 |
Kumar, R | 1 |
Sinha, VR | 1 |
Dahiya, L | 1 |
Sarwal, A | 1 |
Uberall, MA | 1 |
Müller-Schwefe, GH | 1 |
Francis, J | 1 |
Presser, L | 1 |
Malbon, K | 1 |
Braun-Courville, D | 1 |
Linares, LO | 1 |
Schmidt, PJ | 1 |
Ben Dor, R | 1 |
Martinez, PE | 1 |
Guerrieri, GM | 1 |
Harsh, VL | 1 |
Thompson, K | 1 |
Koziol, DE | 1 |
Nieman, LK | 1 |
Rubinow, DR | 1 |
Malmborg, A | 1 |
Persson, E | 1 |
Brynhildsen, J | 1 |
Hammar, M | 1 |
Chung, SJ | 1 |
Asgharnejad, M | 1 |
Bauer, L | 1 |
Ramirez, F | 1 |
Jeon, B | 1 |
Vandenberg, CM | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Retrospective Evaluation of Long Term Use of Oxybutynin in the Pharmacological Treatment of Primary Hyperhidrosis[NCT01956591] | 1,100 participants (Actual) | Observational | 2007-09-30 | Completed | |||
Examining the Effects of Estradiol on Neural and Molecular Response to Rewards in Perimenopausal-Onset Anhedonia and Psychosis[NCT05282277] | Phase 4 | 103 participants (Anticipated) | Interventional | 2022-04-20 | Recruiting | ||
The Effects of Acute Withdrawal of Estradiol on Mood Symptoms in Women With Perimenopausal Depression[NCT00060736] | 60 participants (Actual) | Observational | 2003-05-05 | Completed | |||
Effects of a Tissue Selective Estrogen Complex (TESC) on Depression and the Neural Reward System in the Perimenopause[NCT03740009] | Phase 4 | 20 participants (Actual) | Interventional | 2019-01-02 | Completed | ||
Double Blind, Placebo-controlled, Parallel, Multicenter, Randomized Interventional Phase IV Study to Evaluate the Efficacy of Rotigotine on Depressive Symptoms in Idiopathic Parkinson's Disease Patients[NCT01523301] | Phase 4 | 380 participants (Actual) | Interventional | 2012-04-30 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
"The primary outcome measure is functional magnetic resonance imaging (fMRI) data collected during a Monetary Incentive Delay (MID) Task. All participants will complete the fMRI Monetary Incentive Delay (MID) task at baseline and at 3 weeks. During the task, participants need to select the correct response during win and lose conditions by pressing a button on a button box in the MRI. Participant's blood-oxygen-level dependent (BOLD) activation response (A measurement of oxygen level that is released to neurons since areas of the brain that are thought to be more active or involved in certain tasks require more oxygen to perform the tasks.) is measured while they performed the task in MRI scanner." (NCT03740009)
Timeframe: Baseline to 3 weeks
Intervention | percent signal change (Mean) | |||||
---|---|---|---|---|---|---|
Caudate Baseline | Caudate Posttreatment | Nucleus Accumbens Baseline | Nucleus Accumbens Posttreatment | Putamen Baseline | Putamen Posttreatment | |
Perimenopausal Women, Depressed | .0704 | .0475 | .0623 | .0280 | .0399 | .0408 |
The second primary outcome measure uses the Mood and Anxiety Symptoms Questionnaire - Anhedonic Depression Scale (MASQ-AD) to examine symptom change. All participants will complete the MASQ-AD at each study visit, which measures their current symptoms of depression and anxiety. Scores range from 22 to 110 with lower scores reflecting a better outcome. (NCT03740009)
Timeframe: Baseline, week 2, week 3, week 4 (post treatment)
Intervention | score on a scale (Mean) | |||
---|---|---|---|---|
Baseline Week 1 | Week 2 | Week 3 | Post Treatment Week 4 | |
Perimenopausal Women, Depressed | 72.1 | 62.4 | 57.2 | 54.5 |
The combined score of UPDRS part II and UPDRS part III is the sum of the individual scores and threfore ranges from 0 (normal) to 160 (severe). (NCT01523301)
Timeframe: From Baseline (Week 0) to end of Maintenance Period (up to Week 15)
Intervention | units on a scale (Least Squares Mean) |
---|---|
Efficacy Evaluable Set (Rotigotine Treated Subjects) | -4.20 |
Efficacy Evaluable Set (Placebo Treated Subjects) | -1.81 |
The AS is an abbreviated version of the Apathy Scale (AS). The AS consists of 14 items phrased as questions that are to be answered on a four-point Likert scale. It was developed specifically for patients with Parkinson Disease (PD). For questions 1-8, the scoring system is the following: not at all = 3 points; slightly = 2 points; some =1 point, a lot = 0 point. For questions 9-14: the scoring system is the following: not at all = 0 points; slightly = 1 point; some = 2 points; a lot = 3 points. Adding all scores provides the final score with a range from 0 to 42. (NCT01523301)
Timeframe: From Baseline (Week 0) to end of Maintenance Period (up to Week 15)
Intervention | units on a scale (Least Squares Mean) |
---|---|
Efficacy Evaluable Set (Rotigotine Treated Subjects) | -1.93 |
Efficacy Evaluable Set (Placebo Treated Subjects) | -0.67 |
The Beck Depression Inventory II (BDI-II) is a self-report instrument to measure Depression symptoms and severity. There are 21 items in the BDI-II. Scores of 0-13 are considered minimal depression; 14-19 indicates mild depression; 20-28 indicates moderate depression; and 29-63 indicates severe depression. (NCT01523301)
Timeframe: From Baseline (Week 0) to end of Maintenance Period (up to Week 15)
Intervention | units on a scale (Least Squares Mean) |
---|---|
Efficacy Evaluable Set (Rotigotine Treated Subjects) | -5.87 |
Efficacy Evaluable Set (Placebo Treated Subjects) | -4.68 |
The SHAPS is a self-report instrument developed for the assessment of hedonic capacity. The sum of the 14 items scores ranges from 0 to 14. A higher score represents more anhedonic symptoms. (NCT01523301)
Timeframe: From Baseline (Week 0) to end of Maintenance Period (up to Week 15)
Intervention | units on a scale (Least Squares Mean) |
---|---|
Efficacy Evaluable Set (Rotigotine Treated Subjects) | -0.82 |
Efficacy Evaluable Set (Placebo Treated Subjects) | -0.60 |
The HAM-D consists of 17 items. Nine of the items are scored on a 5-point scale, ranging from 0 to 4. The remaining 8 items are scored on a 3-point scale, from 0 to 2. Therefore, the total score ranges between 0 to 52, with a cutoff score of 15/16 diagnosing major depressive disorder. (NCT01523301)
Timeframe: From Baseline (Week 0) to end of Maintenance Period (up to Week 15)
Intervention | units on a scale (Least Squares Mean) |
---|---|
Efficacy Evaluable Set (Rotigotine Treated Subjects) | -4.79 |
Efficacy Evaluable Set (Placebo Treated Subjects) | -3.68 |
The UPDRS Part II is a tool to measure Activities in Daily Living - it includes speech, salivation, swallowing, handwriting, cutting food and handling utensils, dressing, hygiene, turning in bed and adjusting clothes, falling (unrelated to freezing), freezing when walking, walking, tremor, and sensory complaints related to Parkinsonism. Each of the 13 questions is measured on a scale from 0 (normal) to 4 (severe). The total score of UPDRS part II ranges from 0 (normal) to 52 (severe). (NCT01523301)
Timeframe: From Baseline (Week 0) to end of Maintenance Period (up to Week 15)
Intervention | units on a scale (Least Squares Mean) |
---|---|
Efficacy Evaluable Set (Rotigotine Treated Subjects) | -1.13 |
Efficacy Evaluable Set (Placebo Treated Subjects) | -0.10 |
Improvement of motor symptoms is measured by the change from Baseline in UPDRS Part III motor score. The UPDRS Part III is an accepted and validated scale for the assessment of motor function in Parkinson's disease. Each of the elements in the UPDRS Part III is measured on a scale of 0 to 4, where 0 is normal and 4 represents severe abnormalities. The total score of UPDRS part III ranges from 0 (normal) to 108 (severe abnormalities). (NCT01523301)
Timeframe: From Baseline (Week 0) to end of Maintenance Period (up to Week 15)
Intervention | units on a scale (Least Squares Mean) |
---|---|
Efficacy Evaluable Set (Rotigotine Treated Subjects) | -3.07 |
Efficacy Evaluable Set (Placebo Treated Subjects) | -1.65 |
2 trials available for oxybutynin and Depression
Article | Year |
---|---|
Effects of Estradiol Withdrawal on Mood in Women With Past Perimenopausal Depression: A Randomized Clinical Trial.
Topics: Aged; Cross-Over Studies; Depression; Depressive Disorder; Double-Blind Method; Estradiol; Estrogen | 2015 |
Effects of Estradiol Withdrawal on Mood in Women With Past Perimenopausal Depression: A Randomized Clinical Trial.
Topics: Aged; Cross-Over Studies; Depression; Depressive Disorder; Double-Blind Method; Estradiol; Estrogen | 2015 |
Effects of Estradiol Withdrawal on Mood in Women With Past Perimenopausal Depression: A Randomized Clinical Trial.
Topics: Aged; Cross-Over Studies; Depression; Depressive Disorder; Double-Blind Method; Estradiol; Estrogen | 2015 |
Effects of Estradiol Withdrawal on Mood in Women With Past Perimenopausal Depression: A Randomized Clinical Trial.
Topics: Aged; Cross-Over Studies; Depression; Depressive Disorder; Double-Blind Method; Estradiol; Estrogen | 2015 |
Effects of Estradiol Withdrawal on Mood in Women With Past Perimenopausal Depression: A Randomized Clinical Trial.
Topics: Aged; Cross-Over Studies; Depression; Depressive Disorder; Double-Blind Method; Estradiol; Estrogen | 2015 |
Effects of Estradiol Withdrawal on Mood in Women With Past Perimenopausal Depression: A Randomized Clinical Trial.
Topics: Aged; Cross-Over Studies; Depression; Depressive Disorder; Double-Blind Method; Estradiol; Estrogen | 2015 |
Effects of Estradiol Withdrawal on Mood in Women With Past Perimenopausal Depression: A Randomized Clinical Trial.
Topics: Aged; Cross-Over Studies; Depression; Depressive Disorder; Double-Blind Method; Estradiol; Estrogen | 2015 |
Effects of Estradiol Withdrawal on Mood in Women With Past Perimenopausal Depression: A Randomized Clinical Trial.
Topics: Aged; Cross-Over Studies; Depression; Depressive Disorder; Double-Blind Method; Estradiol; Estrogen | 2015 |
Effects of Estradiol Withdrawal on Mood in Women With Past Perimenopausal Depression: A Randomized Clinical Trial.
Topics: Aged; Cross-Over Studies; Depression; Depressive Disorder; Double-Blind Method; Estradiol; Estrogen | 2015 |
Evaluation of rotigotine transdermal patch for the treatment of depressive symptoms in patients with Parkinson's disease.
Topics: Activities of Daily Living; Aged; Depression; Dopamine Agonists; Double-Blind Method; Female; Humans | 2016 |
10 other studies available for oxybutynin and Depression
Article | Year |
---|---|
The relationship between severity of overactive bladder symptoms and cognitive dysfunction, anxiety and depression in female patients with multiple sclerosis: Running head: OAB-V8, BICAMS and HAD scale in MS.
Topics: Adolescent; Anxiety; Child; Child, Preschool; Cognitive Dysfunction; Depression; Female; Humans; Mul | 2023 |
Influence of antimuscarinic therapy on cognitive functions and quality of life in geriatric patients treated for overactive bladder.
Topics: Activities of Daily Living; Aged; Aged, 80 and over; Benzhydryl Compounds; Benzilates; Benzofurans; | 2015 |
Retrospective evaluation of outcomes in patients with overactive bladder receiving tolterodine versus oxybutynin.
Topics: Benzhydryl Compounds; Comorbidity; Cresols; Delayed-Action Preparations; Depression; Female; Fractur | 2006 |
Oxybutynin for hyperhidrosis.
Topics: Adolescent; Adult; Depression; Female; Glycopyrrolate; Humans; Hyperhidrosis; Male; Mandelic Acids; | 2007 |
Desipramine for interstitial cystitis.
Topics: Adult; Cystitis; Depression; Desipramine; Female; Humans; Mandelic Acids | 1988 |
Transdermal delivery of duloxetine-sulfobutylether-β-cyclodextrin complex for effective management of depression.
Topics: Administration, Cutaneous; Animals; beta-Cyclodextrins; Depression; Duloxetine Hydrochloride; Rats; | 2021 |
[Long-term treatment of chronic pain with low-dose 7-day buprenorphine transdermal patch. Observational data from elderly patients of pain relief and quality of life].
Topics: Activities of Daily Living; Aged; Aged, 80 and over; Anxiety; Buprenorphine; Chronic Pain; Depressio | 2013 |
An exploratory analysis of contraceptive method choice and symptoms of depression in adolescent females initiating prescription contraception.
Topics: Adolescent; Choice Behavior; Contraception; Contraceptive Agents, Female; Contraceptive Devices, Fem | 2015 |
Hormonal contraception and sexual desire: A questionnaire-based study of young Swedish women.
Topics: Adult; Age Factors; Body Mass Index; Contraceptive Agents, Female; Contraceptive Devices, Female; Co | 2016 |
MAOIs and transdermal delivery.
Topics: Antidepressive Agents; Depression; Drug Interactions; Humans; Monoamine Oxidase Inhibitors; Transder | 2012 |