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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 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. The trial reports 2 study locations across 1 state.

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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.

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

FieldValue
Enrollment Target 100 participants
Start Date 2025-08-12
Est. Completion 2026-11
Phase NA

Sponsor

Dartmouth-Hitchcock Medical Center

427 total trials

What the Registry Record Tells You About NCT07041151

The ClinicalTrials.gov registry entry for NCT07041151 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Dartmouth-Hitchcock Medical Center, which has 427 total studies on file at ClinicalTrials.gov.

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 2 study locations spanning 1 distinct geographic area - top geographies include 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.

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