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NCT03522961 · ClinicalTrials.gov registry record · NA
Cranberry Tablets Versus Nitrofurantoin Prophylaxis for Urinary Tract Infection Prevention After Urogynecologic Surgery
A NA study of Urinary Incontinence and Pelvic Organ Prolapse, sponsored by Brigham and Women's Hospital.
- Active
- Registry status
- NA
- Development phase
- 142
- Enrollment target
- 1
- Study location
NCT03522961 is a NA study of Urinary Incontinence and Pelvic Organ Prolapse that is active but no longer recruiting, run by Brigham and Women's Hospital. The registered enrollment target is 142 participants, below the 259-participant average among 48 other Urinary Incontinence trials with a reported enrollment target (45% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03522961, a NA study of Urinary Incontinence and Pelvic Organ Prolapse, is active but no longer recruiting, sponsored by Brigham and Women's Hospital.
- ACTIVE NOT RECRUITING
- Registry status
- NA
- Development phase
- 142 participants
- Enrollment target
- 1
- Study location
Study Summary
We aim to compare the effectiveness of cranberry capsules versus nitrofurantoin prophylaxis in preventing urinary tract infections (UTIs) after urogynecologic surgery by conducting a double-blinded randomized clinical trial involving women with pelvic organ prolapse and/or urinary incontinence scheduled to have surgery with the Urogynecologists who comprise the Brigham and Women's Urogynecology Group.
Conditions Studied
Interventions
- DRUG Nitrofurantoin Prophylaxis/Placebo
- DRUG Cranberry capsules
Study Locations (1)
Massachusetts
- Brigham and Women's Hospital - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 142 participants |
| Start Date | 2018-08-15 |
| Est. Completion | 2026-12-31 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03522961
The ClinicalTrials.gov registry entry for NCT03522961 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 142 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 259-participant average among 48 other Urinary Incontinence trials with a reported enrollment target (45% lower). The listed sponsor is Brigham and Women's Hospital, which has 937 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Urinary Incontinence appearing as the primary indexed condition, and to 2 interventions - of which Nitrofurantoin Prophylaxis/Placebo is the first listed.
NCT03522961 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.
Frequently Asked Questions
What is clinical trial NCT03522961 about?
NCT03522961 is a clinical study titled "Cranberry Tablets Versus Nitrofurantoin Prophylaxis for Urinary Tract Infection Prevention After Urogynecologic Surgery". We aim to compare the effectiveness of cranberry capsules versus nitrofurantoin prophylaxis in preventing urinary tract infections (UTIs) after urogynecologic surgery by conducting a double-blinded randomized clinical trial involving women with pelvic organ prolapse and/or urinary incontinence sched...
What is the current status of trial NCT03522961?
This trial is currently active not recruiting. It is a NA study. The enrollment target is 142 participants. The study started on 2018-08-15. Estimated completion is 2026-12-31.
What conditions does trial NCT03522961 study?
This clinical trial studies the following conditions: Urinary Incontinence, Pelvic Organ Prolapse, Urinary Tract Infections.
What interventions are being tested in trial NCT03522961?
The interventions under investigation include: Nitrofurantoin Prophylaxis/Placebo (DRUG), Cranberry capsules (DRUG).
Who is sponsoring clinical trial NCT03522961?
This trial is sponsored by Brigham and Women's Hospital, which has 937 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03522961 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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