- Trials with a EudraCT protocol (67)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
67 result(s) found for: Neurogenic Bladder.
Displaying page 1 of 4.
EudraCT Number: 2014-004641-27 | Sponsor Protocol Number: UZLeuven | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:UZLeuven | |||||||||||||
Full Title: BOTOX in the treatment of urinary incontinence due to neurogenic detrusor overactivity in patients 3 months - 17 years | |||||||||||||
Medical condition: Urinary incontinence due to neurogenic detrusor overactivity | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004995-20 | Sponsor Protocol Number: 05/SUR/3360E | Start Date*: 2006-06-08 | |||||||||||
Sponsor Name:R and D Department, Cardiff and the Vale NHS Trust | |||||||||||||
Full Title: A Prospective, Single-Arm, Open-label Study to Investigate the Efficacy and Safety of Intravesical Injection of Botulinum Toxin Type-A (500 Units Dysport®) for the Management of Idiopathic Overacti... | |||||||||||||
Medical condition: Idiopathic Overactive bladder syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004996-40 | Sponsor Protocol Number: 04/SUR/3070 | Start Date*: 2006-06-08 | |||||||||||
Sponsor Name:R and D Department, Cardiff and the Vale NHS Trust | |||||||||||||
Full Title: A Prospective, Single-Arm, Open-label Study to Investigate the Efficacy and Safety of Intravesical Injection of Botulinum Toxin Type-A (750 Units Dysport®) for the Management of Neurogenic Detrusor... | |||||||||||||
Medical condition: Neurogenic detrusor overactivity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-004423-11 | Sponsor Protocol Number: 527.66 | Start Date*: 2007-01-22 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: An uncontrolled, open-label, titration, long-term safety (up to 12 months) and efficacy study of tamsulosin hydrochloride in children with neuropathic bladder, with a randomized pharmacokinetic sub... | |||||||||||||
Medical condition: Neurogenic Bladder | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Prematurely Ended) BE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003048-52 | Sponsor Protocol Number: 527.51 | Start Date*: 2007-10-29 | |||||||||||
Sponsor Name:Boehringer Ingelheim Pharma GmbH & Co. KG | |||||||||||||
Full Title: A Phase IIb/III, multi-centre, double-blind, randomised, placebo-controlled, dose ranging study of tamsulosin hydrochloride (low, medium and high dose) as treatment in children with neuropathic bla... | |||||||||||||
Medical condition: Neurogenic Bladder | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002143-83 | Sponsor Protocol Number: 191622-515 | Start Date*: 2006-07-25 | |||||||||||
Sponsor Name:Allergan Ltd | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Study of the Safety and Efficacy of a Single Treatment with Two Dose Levels of BOTOX® (Botulinum Toxin Type A) Purified N... | |||||||||||||
Medical condition: Urinary Incontinence Due to Neurogenic Detrusor Overactivity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) BE (Completed) AT (Completed) CZ (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-006433-13 | Sponsor Protocol Number: TNG-CL008 | Start Date*: 2008-06-11 | ||||||||||||||||
Sponsor Name:Tengion Inc. | ||||||||||||||||||
Full Title: An open-label, multicentre study of augmentation cystoplasty using an autologous Neo-Bladder construct in subjects with spina bifida. | ||||||||||||||||||
Medical condition: Neurogenic bladder secondary to spina bifida | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003407-12 | Sponsor Protocol Number: 191622-518 | Start Date*: 2008-02-19 | |||||||||||
Sponsor Name:Allergan Limited | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Study to Explore the Dose Dependent Response to Three Dose Levels of BOTOX® (Botulinum Toxin Type A) Purified Neurotoxin ... | |||||||||||||
Medical condition: Neurogenic detrusor overactivity as a result of spinal cord injury, in patients with urinary incontinence, who have not been adequately managed with anticholinergic therapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021265-80 | Sponsor Protocol Number: PHRCNATHorsCancer2010-HC11-05 | Start Date*: 2010-10-18 | |||||||||||
Sponsor Name:Centre Hospitalier Universitaire de Reims | |||||||||||||
Full Title: Injections intradétrusoriennes de toxine botulique A chez l'enfant présentant un syndrome d'hyperactivité vésicale neurogène : essai thérapeutique contrôlé multicentrique de non infériorité entre d... | |||||||||||||
Medical condition: Syndrome d'hyperactivité vésicale neurogène chez l'enfant | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021241-44 | Sponsor Protocol Number: PHRI06 – LB / PACHIU | Start Date*: 2010-12-13 | |||||||||||
Sponsor Name:CHRU de TOURS | |||||||||||||
Full Title: Etude multicentrique, randomisée en groupes parallèles, évaluant l’efficacité et la tolérance d’un antibiocycle hebdomadaire dans la prévention des infections urinaires sur vessie neurologique. | |||||||||||||
Medical condition: troubles de la vessie dû à une maladie neurologique | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000192-42 | Sponsor Protocol Number: 191622-516 | Start Date*: 2007-07-25 | |||||||||||
Sponsor Name:Allergan Ltd | |||||||||||||
Full Title: A Multicenter, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group Study of the Safety and Efficacy of a Single Treatment with Two Dose Levels of BOTOX® (Botulinum Toxin Type A) Purified N... | |||||||||||||
Medical condition: Urinary incontinence due to neurogenic detrusor overactivity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) NL (Completed) PT (Completed) ES (Completed) IT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000905-19 | Sponsor Protocol Number: Rec0/0438-IT-CL0491 | Start Date*: 2018-01-29 | |||||||||||
Sponsor Name:Recordati S.p.A | |||||||||||||
Full Title: EFFECTS OF TWO DIFFERENT DOSES OF REC 0/0438 ADMINISTERED BY INTRA-VESICAL INSTILLATION IN PATIENTS WITH NEUROGENIC DETRUSOR OVERACTIVITY DUE TO SPINAL CORD INJURY: A REPEATED DOSES, DOUBLE-BLIND,... | |||||||||||||
Medical condition: neurogenic detrusor overactivity due to spinal cord injury | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) PL (Completed) CZ (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003842-18 | Sponsor Protocol Number: A301223 | Start Date*: 2014-04-24 | |||||||||||||||||||||
Sponsor Name:Erasmus MC | |||||||||||||||||||||||
Full Title: Prevention of renal and bladder damage in children with spina bifida by means of early injections with Botulinum-Toxin-A (Botox): a pilot study. | |||||||||||||||||||||||
Medical condition: Neurogenic bladder function disease in spina bifida patients. | |||||||||||||||||||||||
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Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005455-37 | Sponsor Protocol Number: 178-CL-207 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Astellas Pharma Global Development Inc. | ||||||||||||||||||
Full Title: A Phase 3, Open Label, Multicenter, Baseline-Controlled Sequential Dose Titration Study Followed by a Fixed Dose Observation Period to Evaluate Pharmacokinetics, Efficacy and Safety of Mirabegron P... | ||||||||||||||||||
Medical condition: Neurogenic detrusor overactivity (NDO) | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Ongoing) DK (Ongoing) PL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-009216-53 | Sponsor Protocol Number: 191622-094 | Start Date*: 2009-04-04 | |||||||||||
Sponsor Name:Allergan Ltd | |||||||||||||
Full Title: A Multicenter, Long-term Follow-up Study of the Safety and Efficacy of Two Dose Levels of BOTOX® (Botulinum Toxin Type A) Purified Neurotoxin Complex in Patients with Urinary Incontinence Due to Ne... | |||||||||||||
Medical condition: Urinary incontinence due to neurogenic detrusor overactivity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PT (Completed) NL (Completed) GB (Completed) FR (Completed) DE (Completed) IT (Completed) ES (Completed) BE (Completed) AT (Completed) CZ (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000676-11 | Sponsor Protocol Number: URO-901-3007 | Start Date*: 2022-12-30 | |||||||||||
Sponsor Name:Urovant Sciences GmbH | |||||||||||||
Full Title: A Phase 2/3, Open-label, Baseline-controlled, Multicenter, Long-term Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of Vibegron in Pediatric Subjects 2 Years to < 18 Years of Age with... | |||||||||||||
Medical condition: Neurogenic Detrusor Overactivity (NDO) | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Ongoing) SK (Ongoing) NO (Ongoing) LV (Ongoing) DK (Ongoing) BE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005523-42 | Sponsor Protocol Number: 905-EC-005 | Start Date*: 2007-09-05 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A randomized, double blind, double dummy, placebo controlled study to evaluate the efficacy and safety of solifenacin succinate (5 and 10mg once daily) against placebo and oxybutynin hydrochloride ... | |||||||||||||
Medical condition: Neurogenic detrusor overactivity. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) NL (Completed) GB (Completed) HU (Completed) FR (Completed) DE (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002361-39 | Sponsor Protocol Number: BAY 79-4998 / 12331 | Start Date*: 2006-12-01 | |||||||||||
Sponsor Name:Bayer Vital GmbH | |||||||||||||
Full Title: A 4-week, open-label, multicenter, urodynamic pilot study to explore the efficacy, tolerability and safety of darifenacin (7.5 mg with up-titration to 15 mg) in patients with multiple sclerosis and... | |||||||||||||
Medical condition: Neurogenic overactive bladder disaese in patients with multiple sclerosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000833-36 | Sponsor Protocol Number: STH14330 | Start Date*: 2007-12-14 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: The Action of Botox® on Urgency – A precise evaluation of its impact on urodynamic parameters during bladder filling in patients with non-neurogenic Overactive Bladder (OAB). | |||||||||||||
Medical condition: Non-neurogenic Overactive Bladder (OAB) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000340-15 | Sponsor Protocol Number: 178-CL-202 | Start Date*: 2014-07-11 | ||||||||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | ||||||||||||||||||
Full Title: A multicentre, open-label, single ascending dose Phase 1 study to evaluate the pharmacokinetics, safety and tolerability of mirabegron OCAS tablets in pediatric subjects from 5 to less than 18 year... | ||||||||||||||||||
Medical condition: -neurogenic detrusor overactivity (NDO) -overactive bladder (OAB) | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) BE (Completed) NO (Completed) DK (Completed) | ||||||||||||||||||
Trial results: View results |
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