Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00910845 · ClinicalTrials.gov registry record · Phase 3
Study of Botulinum Toxin Type A for the Treatment of Patients With Idiopathic Overactive Bladder With Urinary Incontinence
A Phase 3 study of Overactive Bladder, sponsored by Allergan.
- Completed
- Registry status
- Phase 3
- Development phase
- 557
- Enrollment target
- 2
- Study locations
NCT00910845 is a Phase 3 study of Overactive Bladder that has completed, run by Allergan. The registered enrollment target is 557 participants, above the 199-participant average among 45 other Overactive Bladder trials with a reported enrollment target (180% higher). The trial reports 2 study locations across 2 states.
The verdict
NCT00910845, a Phase 3 study of Overactive Bladder, has completed, sponsored by Allergan.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 557 participants
- Enrollment target
- 2
- Study locations
Study Summary
The purpose of this study is to assess the safety and effectiveness of botulinum toxin type A (onabotulinumtoxinA) in treating patients with idiopathic overactive bladder with urinary incontinence.
Conditions Studied
Interventions
- DRUG normal saline
- BIOLOGICAL onabotulinumtoxinA
Study Locations (2)
California
- - Newport Beach
British Columbia
- - Victoria
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 557 participants |
| Start Date | 2009-09 |
| Est. Completion | 2011-07 |
| Phase | Phase 3 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00910845
The ClinicalTrials.gov registry entry for NCT00910845 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 557 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 199-participant average among 45 other Overactive Bladder trials with a reported enrollment target (180% higher). The listed sponsor is Allergan, which has 314 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Overactive Bladder appearing as the primary indexed condition, and to 2 interventions - of which normal saline is the first listed.
NCT00910845 reports 2 study locations spanning 2 distinct geographic areas - top geographies include California, British Columbia.
Frequently Asked Questions
What is clinical trial NCT00910845 about?
NCT00910845 is a clinical study titled "Study of Botulinum Toxin Type A for the Treatment of Patients With Idiopathic Overactive Bladder With Urinary Incontinence". The purpose of this study is to assess the safety and effectiveness of botulinum toxin type A (onabotulinumtoxinA) in treating patients with idiopathic overactive bladder with urinary incontinence.
What is the current status of trial NCT00910845?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 557 participants. The study started on 2009-09. Estimated completion is 2011-07.
What conditions does trial NCT00910845 study?
This clinical trial studies the following conditions: Overactive Bladder.
What interventions are being tested in trial NCT00910845?
The interventions under investigation include: normal saline (DRUG), onabotulinumtoxinA (BIOLOGICAL).
Who is sponsoring clinical trial NCT00910845?
This trial is sponsored by Allergan, which has 314 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00910845 being conducted?
This trial has 2 study locations across California, British Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Overactive Bladder
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
Anticholinergic vs. Botox Comparison Study
COMPLETED · Phase 3
-
Behavioral or Solifenacin Therapy for Urinary Symptoms in Parkinson Disease
COMPLETED · Phase 3
-
Home Versus Office Removal of Percutaneous Nerve Evaluation (PNE) Lead
RECRUITING · NA
-
Bladder Botox UTI Antibiotic Prophylaxis
RECRUITING · Phase 4
-
Percutaneous Nerve Evaluation Trial Time
RECRUITING · NA
-
Noninvasive Ultrasound Assessment of Detrusor Dysfunction
RECRUITING
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.