- Trials with a EudraCT protocol (181)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
181 result(s) found for: Urinary incontinence.
Displaying page 1 of 10.
EudraCT Number: 2009-016597-32 | Sponsor Protocol Number: IC-01-01-05-005 | Start Date*: 2010-04-19 | |||||||||||
Sponsor Name:Innovacell Biotechnologie AG | |||||||||||||
Full Title: Skeletal muscle-derived cell implantation in female patients with stress urinary incontinence: a multinational and multicenter open follow-up study | |||||||||||||
Medical condition: Stress urinary incontinence (SUI) in female patients with predominantly intrinsic sphincter deficiency of moderate severity (Grade 2 and Grade 3). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) PL (Ongoing) BG (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012389-30 | Sponsor Protocol Number: Myoblast/ISD/EKS01 | Start Date*: 2009-10-02 | ||||||||||||||||
Sponsor Name:University Medical Centre Ljubljana, Department of Gynaecology | ||||||||||||||||||
Full Title: Transurethral ultrasound-directed injection of autologous myoblasts in combination with functional electrical stimulation in patients with intrinsic urinary sphincter deficiency. | ||||||||||||||||||
Medical condition: Stress urinary incontinence due to intrinsic sphincter deficiency (ISD). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: SI (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000957-30 | Sponsor Protocol Number: 191622-117 | Start Date*: 2012-08-28 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: BOTOX® for the Treatment of Urinary Incontinence due to Neurogenic Detrusor Overactivity in Patients with Multiple Sclerosis | |||||||||||||
Medical condition: Urinary incontinence due to neurogenic detrusor overactivity (NDO) resulting from multiple sclerosis (MS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) PT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014049-10 | Sponsor Protocol Number: HP0749GE201 | Start Date*: 2009-11-27 | |||||||||||
Sponsor Name:Institut de Recherche Pierre Fabre | |||||||||||||
Full Title: Exploratory study of besipirdine efficacy and safety in male patients with persistent stress urinary incontinence after radical prostatectomy | |||||||||||||
Medical condition: Persistant stress urinary incontinence further to radical prostatectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002919-41 | Sponsor Protocol Number: 13-003-05-DE | Start Date*: 2016-12-19 | |||||||||||
Sponsor Name:Cook MyoSite Incorporated | |||||||||||||
Full Title: A Double-blind, Randomized, Controlled Trial Comparing the Safety and Efficacy of AMDC-USR with Placebo in Female Subjects with Stress Urinary Incontinence | |||||||||||||
Medical condition: Female Stress Urinary Incontinence | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000968-16 | Sponsor Protocol Number: F1J-FR-HAAB | Start Date*: 2008-11-18 | |||||||||||
Sponsor Name:CeRePP | |||||||||||||
Full Title: EFFICACY OF DULOXETINE IN THE TREATMENT OF URINARY INCONTINENCEAFTER PROSTATECTOMIE DUE TO CANCER | |||||||||||||
Medical condition: We want to evaluate the effect of Duloxetine 40mg BID (80mg daily dose) on the number of urinary incontinence episodes as shown on a 74 days bladder diary, compared to placebo for male which had a... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004898-30 | Sponsor Protocol Number: 191622-121 | Start Date*: 2013-07-18 | |||||||||||
Sponsor Name:Allergan Ltd | |||||||||||||
Full Title: Long-term Extension Study of BOTOX® in the Treatment of Urinary Incontinence Due to Neurogenic Detrusor Overactivity in Patients 5 to 17 Years of Age | |||||||||||||
Medical condition: Urinary Incontinence due to Neurogenic Detrusor Overactivity | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) AT (Completed) IT (Completed) DE (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005350-21 | Sponsor Protocol Number: A0221064 | Start Date*: 2009-02-03 | |||||||||||
Sponsor Name:Pfizer Limited, Ramsgate Road, Sandwich, Kent CT13 9NJ, UK | |||||||||||||
Full Title: A PHASE 2, RANDOMIZED, DOUBLE-BLIND, MULTI-DOSE, PLACEBO-CONTROLLED CROSSOVER STUDY OF THE EFFICACY OF FESOTERODINE IN INCREASING URETHRAL PRESSURE IN STRESS URINARY INCONTINENCE PATIENTS | |||||||||||||
Medical condition: Stress urinary incontinence | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001656-34 | Sponsor Protocol Number: IC-01-01-05-015 | Start Date*: 2014-10-01 | |||||||||||
Sponsor Name:Innovacell Biotechnologie AG | |||||||||||||
Full Title: Skeletal muscle-derived cell implantation in female patients with stress urinary incontinence: a multinational and multicenter open follow-up study | |||||||||||||
Medical condition: Stress urinary incontinence (SUI) in female patients of moderate severity (Grade 2 and Grade 3) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020944-37 | Sponsor Protocol Number: 09/0127 | Start Date*: 2011-10-31 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: Pilot study to establish laboratory methods for urine Nerve Growth Factor (NGF) and immunohistochemical staining of the vanilloid receptor (TRPV1) in bladder biopsies, following open label treatmen... | |||||||||||||
Medical condition: Neurogenic & Idiopathic detrusor overactivity in the bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011797-15 | Sponsor Protocol Number: IC-01-01-4-003 | Start Date*: 2009-12-18 | |||||||||||
Sponsor Name:Innovacell Biotechnologie AG | |||||||||||||
Full Title: Skeletal muscle-derived cell implantation in female patients with stress urinary incontinence: a multicenter, randomized, parallel-group, placebo-controlled clinical study | |||||||||||||
Medical condition: Stress urinary incontinence (SUI) in female patients with predominately intrinsic sphincter deficiency of moderate severity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001559-12 | Sponsor Protocol Number: A6061024 | Start Date*: 2005-08-01 | |||||||||||
Sponsor Name:Pfizer | |||||||||||||
Full Title: Measurement of Urethral Function in Women with Stress Urinary Incontinence - Evaluation of the Sensitivity of Urethral Reflectometry compared to Urethral Pressure Profilometry, using [S,S]-Reboxeti... | |||||||||||||
Medical condition: Stress Urinary Incontinence (SUI) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021867-34 | Sponsor Protocol Number: IC-01-01-5-006 | Start Date*: 2011-12-07 | |||||||||||
Sponsor Name:Innovacell Biotechnologie AG - Life Science Center Innsbruck | |||||||||||||
Full Title: An open, multicenter study to evaluate the urodynamic properties of a local implantation of autologous skeletal muscle-derived cells (SMDCs) in female patients with stress urinary incontinence | |||||||||||||
Medical condition: Stress urinary incontinence (SUI) in female patients with predominantly intrinsic sphincter deficiency of moderate severity (Grade 2 and Grade 3) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: SI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000476-13 | Sponsor Protocol Number: SP738 | Start Date*: 2004-08-10 |
Sponsor Name:Schwarz Biosciences GmbH | ||
Full Title: LONG-TERM OPEN-LABEL EXTENSION TRIAL FOR SUBJECTS COMPLETING THE PHASE 3 TRIAL OF FESOTERODINE (SP583) FOR THE TREATMENT OF OVERACTIVE BLADDER SYNDROME | ||
Medical condition: overactive bladder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-006299-39 | Sponsor Protocol Number: 191622-082-01 | Start Date*: 2008-04-23 | |||||||||||
Sponsor Name:Allergan | |||||||||||||
Full Title: A Placebo-Controlled, Randomized, Safety and Efficacy Study of BOTOX® (Botulinum Toxin Type A) Purified Neurotoxin Complex in Patients with Neurogenic Detrusor Overactivity and Neurological Respira... | |||||||||||||
Medical condition: Patients with urinary incontinence due to neurogenic detrusor overactivity as a result of spinal cord injury or multiple sclerosis who have not been adequately managed with anticholinergic therapy ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000464-17 | Sponsor Protocol Number: 191622-137 | Start Date*: 2014-06-17 | |||||||||||
Sponsor Name:Allergan Limited | |||||||||||||
Full Title: BOTOX® in the Treatment of Urinary Incontinence Due to Overactive Bladder in Patients 12 to 17 Years of Age | |||||||||||||
Medical condition: Urinary Incontinence Due to Overactive Bladder | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) BE (Completed) IT (Prematurely Ended) NL (Prematurely Ended) NO (Completed) PL (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004877-26 | Sponsor Protocol Number: 191622-120 | Start Date*: 2013-07-18 | |||||||||||
Sponsor Name:Allergan Ltd. | |||||||||||||
Full Title: BOTOX® in the Treatment of Urinary Incontinence Due to Neurogenic Detrusor Overactivity in Patients 5 to 17 Years of Age | |||||||||||||
Medical condition: Urinary Incontinence Due to Neurogenic Detrusor Overactivity | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) AT (Completed) IT (Completed) DE (Completed) PL (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-006201-12 | Sponsor Protocol Number: 003 | Start Date*: 2007-01-10 | |||||||||||
Sponsor Name:MERCK SHARP DOHME | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Placebo- and Active-Controlled, Parallel-Group, Dose-Ranging Study of MK-0594 in Patients With Overactive Bladder | |||||||||||||
Medical condition: overactove bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021871-10 | Sponsor Protocol Number: IC-01-01-05-004 | Start Date*: 2012-04-18 | |||||||||||
Sponsor Name:Innovacell Biotechnologie AG - Life Science Center Innsbruck | |||||||||||||
Full Title: A multicenter, randomized, double-blinded, parallel-group, placebocontrolled study to assess the efficacy and safety of skeletal muscle-derived cell implantation in female patients with stress urin... | |||||||||||||
Medical condition: Stress urinary incontinence (SUI) of moderate severity (Grade 2 and Grade 3) in female patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) CZ (Completed) BG (Completed) AT (Completed) IT (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004036-36 | Sponsor Protocol Number: 178-MA-1008 | Start Date*: 2016-07-18 | |||||||||||
Sponsor Name:Astellas Pharma Global development, Inc | |||||||||||||
Full Title: A Phase 4, Double-Blind, Randomized, Placebo-controlled, Multi- Center Study to Evaluate the Efficacy, Safety, and Tolerability of Mirabegron in Men with Overactive Bladder (OAB) Symptoms While ... | |||||||||||||
Medical condition: Over active bladder (OAB) in men with Lower Urinary Tract Symptoms (LUTS) due to Benign Prostatic Hyperplasia (BPH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) PL (Completed) ES (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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