- Trials with a EudraCT protocol (3)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3 result(s) found for: Dyssynergia.
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EudraCT Number: 2005-001378-29 | Sponsor Protocol Number: RAE02 | Start Date*: 2005-05-23 |
Sponsor Name:Bradford Teaching Hospitals NHS Foundation Trust | ||
Full Title: A double blinded randomised controlled trial of injection of botulinum toxin versus normal saline into the puborectalis muscle in patients with pelvic floor dyssynergia. | ||
Medical condition: Obstructed defeacation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003357-85 | Sponsor Protocol Number: FRI200701 | Start Date*: 2007-10-10 | |||||||||||
Sponsor Name:ISTITUTO NEUROLOGICO "CARLO BESTA" | |||||||||||||
Full Title: Randomized placebo-controlled double-blind trial to assess safety and efficacy of erythropoietin in adult patients with Friedreich's ataxia (a pilot study) | |||||||||||||
Medical condition: Friedreich ataxia (FRDA) is a rare autosomal recessive neurodegenerative disorder caused a mutation in the FXN gene, which encodes a protein named frataxin. As a result of the mutation, frataxin is... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-013334-24 | Sponsor Protocol Number: KN0203Y-001 | Start Date*: 2010-01-08 | ||||||||||||||||
Sponsor Name:KeyNeurotek Pharma GmbH | ||||||||||||||||||
Full Title: Double-blind placebo-controlled proof of concept study with the ยต-receptor agonist KN203 in patients with overactive bladder syndrome Double-blind, randomized, parallel groups prospective phase II-... | ||||||||||||||||||
Medical condition: Women with urgency-frequency syndrome with urinary incontinence due to detrusor instability diagnosed by cystometry. oder Patients with overactive bladder with or without urinary urge incontinenc... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
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