Viewing Study NCT04635566


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Study NCT ID: NCT04635566
Status: COMPLETED
Last Update Posted: 2020-11-19
First Post: 2020-11-14
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Pharmacological Enhancement for Nocturnal Incontinence in Orthotopic Bladder Substitute
Sponsor: Mansoura University
Organization:

Study Overview

Official Title: Pharmacological Enhancement for Nocturnal Incontinence in Orthotopic Bladder Substitute. A Randomised Controlled Trial
Status: COMPLETED
Status Verified Date: 2020-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: In this randomised trial, we hypothesised that mebeverine could enhance nocturnal continenece of Orthotopic Bladder Substitute (OBS) patients by decreasing the frequency and reduce maximum amplitude of uninhibited contractions of OBS ileum, and consequently it would increase the OBS capacity
Detailed Description: None

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: