- Trials with a EudraCT protocol (120)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
120 result(s) found for: Micturition.
Displaying page 1 of 6.
EudraCT Number: 2004-002397-38 | Sponsor Protocol Number: EFC5722 | Start Date*: 2007-09-03 | |||||||||||
Sponsor Name:sanofi-aventis recherche et développement | |||||||||||||
Full Title: 12-week, multicenter, double-blind, randomized, placebo-controlled, parallel-group study to investigate the efficacy, pharmacodynamic and safety of two doses of alfuzosin (0.1 mg/kg/day; 0.2 mg/kg/... | |||||||||||||
Medical condition: Children with voiding dysfunction of neuropathic etiology | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) PT (Completed) DE (Completed) ES (Completed) PL (Completed) EE (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001451-19 | Sponsor Protocol Number: 178-CL-046 | Start Date*: 2008-06-05 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A Randomized, Double-blind, Parallel Group, Placebo and Active Controlled, Multicenter Study to Assess the Efficacy and Safety of the Beta-3 Agonist YM178 (50 mg qd and 100 mg qd) in Subjects with ... | |||||||||||||
Medical condition: Symptoms of Overactive Bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) SE (Completed) IS (Completed) CZ (Completed) LV (Completed) IE (Completed) GB (Completed) BE (Completed) FR (Completed) ES (Completed) HU (Completed) DK (Completed) LT (Completed) PT (Completed) IT (Completed) NL (Completed) AT (Completed) GR (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000983-26 | Sponsor Protocol Number: EFC6269 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:sanofi-aventis recherche et développement | |||||||||||||
Full Title: 12-week, multicenter, open-label, non-comparative study to investigate pharmacodynamic and safety of alfuzosin 0.2 mg/kg/day in the treatment of children and adolescents 2 - 16 years of age with hy... | |||||||||||||
Medical condition: Children with voiding dysfunction of neuropathic etiology | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) EE (Completed) BG (Completed) SK (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-007087-42 | Sponsor Protocol Number: 178-CL-074 | Start Date*: 2009-06-03 |
Sponsor Name:Astellas Pharma Europe B.V. | ||
Full Title: A Phase III, Randomized, Double-Blind, Parallel Group, Placebo Controlled, Multicenter Study to Assess the Efficacy and Safety of the Beta-3 Agonist YM178 (25 mg qd and 50 mg qd) in Subjects with ... | ||
Medical condition: Symptoms of overactive bladder | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) FI (Completed) PT (Completed) ES (Completed) DE (Completed) SE (Completed) DK (Completed) HU (Completed) SK (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005546-39 | Sponsor Protocol Number: 905-EC-003 | Start Date*: 2006-12-11 |
Sponsor Name:Astellas Pharma Europe BV | ||
Full Title: SOLIFENACIN SUCCINATE IN A FLEXIBLE DOSE REGIMEN WITH SIMPLIFIED BLADDER TRAINING VERSUS SOLIFENACIN SUCCINATE IN A FLEXIBLE DOSE REGIMEN ALONE IN A PROSPECTIVE, RANDOMIZED, PARALLEL GROUP, OVERACT... | ||
Medical condition: Solifenacin succinate is indicated for the relief of symptoms of urinary frequency, nocturia and urgency with or without incontinence, associated with overactive bladder 10059617 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) IE (Completed) HU (Completed) CZ (Completed) GB (Completed) DK (Completed) SE (Completed) IT (Completed) FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-020601-32 | Sponsor Protocol Number: 178-CL-100 | Start Date*: 2011-03-23 | |||||||||||
Sponsor Name:Astellas Pharma Europe BV | |||||||||||||
Full Title: A Randomized, Double-Blind, Factorial, Parallel-Group, Active and Placebo-Controlled, Multicenter Dose-Ranging Study to Evaluate the Efficacy, Safety and Tolerability of Six Dose Combinations of So... | |||||||||||||
Medical condition: Overactive Bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) GB (Completed) SE (Completed) FI (Completed) HU (Completed) CZ (Completed) DK (Completed) SK (Completed) PT (Completed) NO (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001243-30 | Sponsor Protocol Number: 840 30 40 | Start Date*: 2004-12-09 |
Sponsor Name:Apogepha Arzneimittel GmbH | ||
Full Title: Propiverine hydrochloride in children suffering from overactive bladder and urinary incontinence. A randomised, double-blind, placebo-controlled, parallel grouped multicentre clinical trial. | ||
Medical condition: children suffering from overactive bladder and urinary incontinence | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: CZ (Completed) SK (Completed) AT (Completed) SE (Completed) NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001452-39 | Sponsor Protocol Number: 178-CL-049 | Start Date*: 2008-06-05 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A Randomized, Double-Blind, Parallel Group, Active Controlled, Multicenter Long-term Study to Assess the Safety and Efficacy of the Beta-3 Agonist YM178 (50 mg qd and 100 mg qd) in Subjects with Sy... | |||||||||||||
Medical condition: Symptoms of overactive bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) SE (Completed) IS (Completed) CZ (Completed) LV (Completed) IE (Completed) GB (Completed) BE (Completed) FR (Completed) ES (Completed) DK (Completed) LT (Completed) SK (Completed) PT (Completed) NL (Completed) IT (Completed) HU (Completed) AT (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001211-37 | Sponsor Protocol Number: 905-CL-055 | Start Date*: 2009-07-16 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A randomized, double-blind, parallel group, placebo controlled, multi-center study of fixed dose combinations of solifenacin succinate (6 mg and 9 mg) with tamsulosin hydrochloride OCAS 0.4 mg and ... | |||||||||||||
Medical condition: Lower urinary tract symptoms (LUTS) associated with benign prostatic hyperplasia (BPH). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Completed) FR (Completed) SK (Completed) AT (Completed) BE (Completed) IT (Completed) DE (Completed) HU (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002256-17 | Sponsor Protocol Number: 178-CL-044 | Start Date*: 2006-01-19 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A Randomized, Double-blind, Parallel Group, Placebo and Active Controlled, Multi-Center Dose Ranging Study with the Beta-3 AGONist YM178 in Patients with Symptomatic Overactive Bladder (DRAGON) | |||||||||||||
Medical condition: Overactive bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) CZ (Completed) DE (Completed) ES (Completed) SE (Completed) BE (Completed) HU (Completed) DK (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001119-69 | Sponsor Protocol Number: ESCLIN-003/04 | Start Date*: 2004-11-03 |
Sponsor Name:Laboratorios Dr. Esteve, SA | ||
Full Title: An evaluation of the dose-response relationship of Cizolirtine citrate 300 mg, twice daily, and 400 mg, twice daily, versus placebo in subjects with urge urinary incontinence. A 12-week, randomised... | ||
Medical condition: Urge Urinary Incontinence | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Ongoing) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001268-57 | Sponsor Protocol Number: 905-CL-058 | Start Date*: 2007-09-12 | ||||||||||||||||
Sponsor Name:Astellas Pharma US, Inc. | ||||||||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Parallel Group, Placebo Controlled, Multi-Center Study to Evaluate the Safety of the Co-administration of Solifenacin Succinate with 0.4 mg Tamsulosin Hydrochlo... | ||||||||||||||||||
Medical condition: Storage and Voiding Lower Urinary Tract Symptoms (LUTS) and Bladder Outlet Obstruction (BOO) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
Trial protocol: CZ (Completed) BE (Completed) HU (Completed) DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-007087-17 | Sponsor Protocol Number: A0221045 | Start Date*: 2008-06-13 | |||||||||||
Sponsor Name:Pfizer Limited, Ramsgate Road, Sandwich, Kent, UK | |||||||||||||
Full Title: A 24-WEEK, MULTICENTRE TRIAL, COMPRISING A 12-WEEK, RANDOMISED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL-GROUP PHASE FOLLOWED BY A 12-WEEK OPEN-LABEL PHASE, TO EVALUATE THE EFFICACY AND SAFETY OF... | |||||||||||||
Medical condition: Treatment of overactive bladder with symptoms of frequency, urgency, and urgency incontinence (Some patients will also have urgency urinary incontinence (UUI)). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) GB (Completed) BE (Completed) SK (Completed) AT (Completed) DE (Completed) DK (Completed) PT (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004555-11 | Sponsor Protocol Number: A0221009 | Start Date*: 2008-01-23 | |||||||||||
Sponsor Name:Pfizer Inc. 235 East 42nd Street, NEW YORK, NY 10017. US | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY TO EVALUATE THE EFFICACY AND SAFETY OF FESOTERODINE AS AN "ADD-ON" THERAPY IN MEN WITH PERSISTENT OVERACTIVE BLADDER SYMPTOMS UNDER MONOTHERAPY ... | |||||||||||||
Medical condition: overactive bladder (OAB) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) BE (Completed) NL (Completed) GR (Completed) SK (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024181-22 | Sponsor Protocol Number: A0221095 | Start Date*: 2011-05-18 | |||||||||||
Sponsor Name:Pfizer Inc.235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A 12-WEEK, PHASE 4, RANDOMIZED, DOUBLE-BLIND, PLACEBO CONTROLLED, PARALLEL GROUP, MULTICENTER TRIAL IN OVERACTIVE BLADDER SUBJECTS TO CONFIRM THE EFFICACY OF 8 MG FESOTERODINE COMPARED TO 4 MG F... | |||||||||||||
Medical condition: Overactive Bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) CZ (Completed) HU (Completed) DE (Completed) FI (Completed) GR (Completed) LT (Completed) AT (Completed) DK (Completed) SK (Completed) BG (Prematurely Ended) NO (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006070-22 | Sponsor Protocol Number: A0221007 | Start Date*: 2007-03-16 | |||||||||||
Sponsor Name:Pfizer Inc | |||||||||||||
Full Title: A 12-WEEK, MULTICENTER, OPEN-LABEL, SINGLE-ARM STUDY TO EVALUATE THE EFFECTS OF FESOTERODINE ON TREATMENT SATISFACTION AND SYMPTOM RELIEF IN OVERACTIVE BLADDER PATIENTS | |||||||||||||
Medical condition: Overactive bladder (OAB) is a symptom complex defined by the International Continence Society (ICS) as the symptoms of urgency, with or without urgency incontinence, usually with frequency and noct... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) SK (Completed) CZ (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005344-15 | Sponsor Protocol Number: BOTC3-OAB-01 | Start Date*: 2013-03-25 | |||||||||||
Sponsor Name:Adyton, s.r.o. | |||||||||||||
Full Title: A Double Blind Study Aiming To Evaluate The Efficacy Of Bladder Instillation With Botulinum Toxin (200U) + TC-3 Gel In Comparison To Instillation With Botulinum Toxin (200U) + TC-3 Gel + DMSO, To D... | |||||||||||||
Medical condition: Overactive bladder (OAB) syndrome (in women), as defined by the International Continence Society (ICS): severe urgency with or without urge urinary incontinence, usually accompanied with increased ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-003135-30 | Sponsor Protocol Number: URO-901-3005 | Start Date*: 2019-12-12 | |||||||||||
Sponsor Name:Urovant Sciences GmbH | |||||||||||||
Full Title: A Phase 3 Double-Blind, Randomized, Placebo-Controlled, Multi-Center Study to Evaluate the Efficacy, Safety and Tolerability of Vibegron in Men with Overactive Bladder (OAB) Symptoms on Pharmacolog... | |||||||||||||
Medical condition: Overactive Bladder (OAB) in men with Benign Prostatic Hyperplasia (BPH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: LT (Completed) ES (Ongoing) HU (Completed) PT (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002999-34 | Sponsor Protocol Number: Y-79-52120-126 | Start Date*: 2007-12-04 | |||||||||||
Sponsor Name:Ipsen Limited | |||||||||||||
Full Title: A phase II, international, multi-centre, prospective, randomised, parallel-group, double-blind, dose-ranging, placebo-controlled, 12-week, princeps study to assess the efficacy and safety of a one ... | |||||||||||||
Medical condition: Idiopathic overactive bladder | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Prematurely Ended) NL (Prematurely Ended) BE (Completed) FR (Completed) CZ (Completed) IT (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005145-11 | Sponsor Protocol Number: BAY 38-9456 / 12392 | Start Date*: 2007-07-27 | |||||||||||
Sponsor Name:Bayer Healthcare AG | |||||||||||||
Full Title: Randomized, double-blind, placebo-controlled, parallel group study of vardenafil 10 mg twice daily to assess the effect on urodynamics in patients with Overactive Bladder (detrusor overactivity). | |||||||||||||
Medical condition: Overactive bladder (detrusor overactivity) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) PT (Completed) ES (Completed) HU (Completed) CZ (Completed) BE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
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