- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: Bladder sphincter.
Displaying page 1 of 1.
| EudraCT Number: 2008-004858-33 | Sponsor Protocol Number: Version 2.0 (03Nov2010) | Start Date*: 2009-01-09 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: Open label pilot study to treat women with chronic urinary retention or voiding dysfunction due to a primary disorder of sphincter relaxation (Fowler’s syndrome) with outpatient urethral sphincter ... | |||||||||||||
| Medical condition: Primary abnormality of the urethral sphincter or Fowlers Syndrome | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003949-28 | Sponsor Protocol Number: Inco_Ona1 | Start Date*: 2018-08-07 | |||||||||||
| Sponsor Name:PROF. ANTONELLA GIANNANTONI - CLINICA UROLOGICA - UNIVERSITà DI PERUGIA | |||||||||||||
| Full Title: Incobotulinumtoxin versus Onabotulinumtoxin in the treatment of patients with overactive bladder syndrome | |||||||||||||
| Medical condition: neurogenic overactive bladder | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| 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: 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: 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: 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 (Completed) BG (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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