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NCT07041151 · ClinicalTrials.gov registry record · NA
Self-discontinuation of Urinary Catheters in a Rural Population
A NA study of Post-Operative Urinary Retention, sponsored by Dartmouth-Hitchcock Medical Center.
- Recruiting
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 2
- Study locations
NCT07041151: Recruiting NA study of Post-Operative Urinary Retention, sponsored by Dartmouth-Hitchcock Medical Center.
NCT07041151 is a NA study of Post-Operative Urinary Retention that is actively recruiting participants, run by Dartmouth-Hitchcock Medical Center. The registered enrollment target is 100 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07041151, a NA study of Post-Operative Urinary Retention, is actively recruiting participants, sponsored by Dartmouth-Hitchcock Medical Center.
- RECRUITING
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 2
- Study locations
Study Summary
The goal of this study is to understand patient satisfaction with two different ways of managing difficulty urinating after gynecologic surgery with a focus on those patients who receive care in a rural area. One common practice is to have an "office catheter removal." This means, if a patient has trouble urinating after surgery and goes home with a foley catheter, they usually have to come back to the clinic within 2-3 days to have the catheter removed and to do a test to see if they can urinate on their own. For some patients, coming back to the clinic so soon after surgery can be difficult, especially for those patients who live far away or are dependent on others for getting to appointments. A second, less common, practice is to have patients remove their own catheter at home, or "self-removal of urinary (Foley) catheter." With self-removal, patients remove their Foley catheter at home, and confirm that they are urinating normally. This approach has been shown to be safe, with similar patient satisfactions, and success, but those studies did not take into account situations where patients may live a rural area and/or travel a long distance to the medical center to receive care. This study is comparing the in-office removal with self-removal. The goal is to find out which option patients prefer, how convenient each approach is, and how well they work. The main goal of this study is to understand patient satisfaction and improve care after surgery.
Conditions Studied
Interventions
- OTHER At-home Foley Catheter Self-Removal with Passive Void Trial
- OTHER In-Office Foley Catheter Removal and Backfill Void Trial
Study Locations (2)
New Hampshire
- Dartmouth Hitchcock Medical Center - Lebanon
- Dartmouth Manchester Ambulatory Surgery Center - Manchester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2025-08-12 |
| Est. Completion | 2026-11 |
| Phase | NA |
What NCT07041151 shows while recruiting
NCT07041151 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).
The record links to 1 condition, with Post-Operative Urinary Retention appearing as the primary indexed condition, and to 2 interventions - of which At-home Foley Catheter Self-Removal with Passive Void Trial is the first listed.
NCT07041151 reports a single indexed study location in New Hampshire.
Frequently Asked Questions
What is clinical trial NCT07041151 about?
NCT07041151 is a clinical study titled "Self-discontinuation of Urinary Catheters in a Rural Population". The goal of this study is to understand patient satisfaction with two different ways of managing difficulty urinating after gynecologic surgery with a focus on those patients who receive care in a rural area. One common practice is to have an "office catheter removal." This means, if a patient has ...
What is the current status of trial NCT07041151?
This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2025-08-12. Estimated completion is 2026-11.
What conditions does trial NCT07041151 study?
This clinical trial studies the following conditions: Post-Operative Urinary Retention.
What interventions are being tested in trial NCT07041151?
The interventions under investigation include: At-home Foley Catheter Self-Removal with Passive Void Trial (OTHER), In-Office Foley Catheter Removal and Backfill Void Trial (OTHER).
Who is sponsoring clinical trial NCT07041151?
This trial is sponsored by Dartmouth-Hitchcock Medical Center, which has 427 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07041151 being conducted?
This trial has 2 study locations across New Hampshire. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT07041151's enrollment target sits among peer trials
100 840th of 2000 higher than 1,081 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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