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NCT03043287

Voiding Efficiency, a Predictor of Clean Intermittent Catheterization (CIC)

Completed Last updated 5 February 2020
What this trial tests

trial testing onabotulinumtoxinA in Urinary Bladder, Overactive in 420 participants. Completed in 30 September 2019.

Timeline
12 May 2017
Primary endpoint
9 September 2019
30 September 2019

Quick facts

Lead sponsorAllergan
StatusCompleted
Study typeOBSERVATIONAL
Enrollment420
Start date12 May 2017
Primary completion9 September 2019
Estimated completion30 September 2019
Sites3 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Allergan — full company profile →

Who can join

18 and older, any sex, with Urinary Bladder, Overactive. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is a retrospective chart review of patients treated with onabotulinumtoxinA (BOTOX®) for idiopathic overactive bladder (OAB) and will determine voiding efficiency (VE) cutoff ratios that predict post-procedure urinary retention requiring catheterization.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of onabotulinumtoxinA

Trials testing the same drug.

Other recruiting trials for Urinary Bladder, Overactive

Currently open trials in the same condition.

Other Allergan trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03043287.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing