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NCT03898310 · ClinicalTrials.gov registry record · NA
UTI Prophylaxis With Cranberry Extract After Female Incontinence Surgery
A NA study of Urinary Tract Infections and Incontinence, sponsored by University of Oklahoma.
- Completed
- Registry status
- NA
- Development phase
- 141
- Enrollment target
- 1
- Study location
NCT03898310 is a NA study of Urinary Tract Infections and Incontinence that has completed, run by University of Oklahoma. The registered enrollment target is 141 participants, below the 454-participant average among 34 other Urinary Tract Infections trials with a reported enrollment target (69% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03898310, a NA study of Urinary Tract Infections and Incontinence, has completed, sponsored by University of Oklahoma.
- COMPLETED
- Registry status
- NA
- Development phase
- 141 participants
- Enrollment target
- 1
- Study location
Study Summary
The risk of urinary tract infection (UTI) following female incontinence surgery ranges between 6-48%. The literature has shown mixed results of the therapeutic efficacy of cranberry extract to prevent UTI in females, with some promising preliminary work in the prevention of UTI's following gynecologic surgery. The researchers will conduct a study of the effect of cranberry extracts on preventing urinary tract infections following mid urethral slings, which are the most common urinary incontinence procedures.
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Placebo capsule
- DIETARY_SUPPLEMENT Cranberry extract capsules
Study Locations (1)
Oklahoma
- University of Oklahoma - Oklahoma City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 141 participants |
| Start Date | 2019-02-05 |
| Est. Completion | 2023-01-22 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03898310
The ClinicalTrials.gov registry entry for NCT03898310 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 141 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 454-participant average among 34 other Urinary Tract Infections trials with a reported enrollment target (69% lower). The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Urinary Tract Infections appearing as the primary indexed condition, and to 2 interventions - of which Placebo capsule is the first listed.
NCT03898310 reports 1 study location spanning 1 distinct geographic area - top geographies include Oklahoma.
Frequently Asked Questions
What is clinical trial NCT03898310 about?
NCT03898310 is a clinical study titled "UTI Prophylaxis With Cranberry Extract After Female Incontinence Surgery". The risk of urinary tract infection (UTI) following female incontinence surgery ranges between 6-48%. The literature has shown mixed results of the therapeutic efficacy of cranberry extract to prevent UTI in females, with some promising preliminary work in the prevention of UTI's following gynecolog...
What is the current status of trial NCT03898310?
This trial is currently completed. It is a NA study. The enrollment target is 141 participants. The study started on 2019-02-05. Estimated completion is 2023-01-22.
What conditions does trial NCT03898310 study?
This clinical trial studies the following conditions: Urinary Tract Infections, Incontinence.
What interventions are being tested in trial NCT03898310?
The interventions under investigation include: Placebo capsule (DIETARY_SUPPLEMENT), Cranberry extract capsules (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT03898310?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03898310 being conducted?
This trial has 1 study location across Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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