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NCT04232683 · ClinicalTrials.gov registry record · Early Phase 1
Preoperative Tamsulosin to Prevent Postoperative Urinary Retention After Surgery For Pelvic Floor Disorders
A Early Phase 1 study of Urinary Retention, sponsored by The Cleveland Clinic.
- Active
- Registry status
- Early Phase 1
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT04232683 is a Early Phase 1 study of Urinary Retention that is active but no longer recruiting, run by The Cleveland Clinic. The registered enrollment target is 100 participants, below the 131-participant average among 11 other Urinary Retention trials with a reported enrollment target (24% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04232683, a Early Phase 1 study of Urinary Retention, is active but no longer recruiting, sponsored by The Cleveland Clinic.
- ACTIVE NOT RECRUITING
- Registry status
- Early Phase 1
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
Our hypothesis is that patients receiving preoperative Tamsulosin will have decrease rates of postoperative urinary retention (POUR) after surgery in females for pelvic floor disorders.
Conditions Studied
Interventions
- DRUG Placebo oral tablet
- DRUG Tamsulosin 0.4Mg Capsule
Study Locations (1)
Florida
- Cleveland Clinic Florida - Weston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2019-12-18 |
| Est. Completion | 2025-12 |
| Phase | Early Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04232683
The ClinicalTrials.gov registry entry for NCT04232683 describes a study currently listed as active not recruiting, categorized as Early Phase 1. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 131-participant average among 11 other Urinary Retention trials with a reported enrollment target (24% lower). The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Urinary Retention appearing as the primary indexed condition, and to 2 interventions - of which Placebo oral tablet is the first listed.
NCT04232683 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT04232683 about?
NCT04232683 is a clinical study titled "Preoperative Tamsulosin to Prevent Postoperative Urinary Retention After Surgery For Pelvic Floor Disorders". Our hypothesis is that patients receiving preoperative Tamsulosin will have decrease rates of postoperative urinary retention (POUR) after surgery in females for pelvic floor disorders.
What is the current status of trial NCT04232683?
This trial is currently active not recruiting. It is a Early Phase 1 study. The enrollment target is 100 participants. The study started on 2019-12-18. Estimated completion is 2025-12.
What conditions does trial NCT04232683 study?
This clinical trial studies the following conditions: Urinary Retention.
What interventions are being tested in trial NCT04232683?
The interventions under investigation include: Placebo oral tablet (DRUG), Tamsulosin 0.4Mg Capsule (DRUG).
Who is sponsoring clinical trial NCT04232683?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04232683 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Read our methodology - how this data is sourced, computed, and verified.
Related
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