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NCT03753516 · ClinicalTrials.gov registry record · NA
Pelvic Floor Support After Laparoscopic Hysterectomy for Benign Conditions: A Randomized Controlled Trial Comparing Vaginal Cuff Closure Techniques
A NA study, sponsored by Walter Reed National Military Medical Center.
- Terminated
- Registry status
- NA
- Development phase
- 58
- Enrollment target
NCT03753516: Clinical Trial NA study, sponsored by Walter Reed National Military Medical Center.
NCT03753516 is a NA study that was terminated before completion, run by Walter Reed National Military Medical Center. The registered enrollment target is 58 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03753516, a NA study, was terminated before completion, sponsored by Walter Reed National Military Medical Center.
- TERMINATED
- Registry status
- NA
- Development phase
- 58 participants
- Enrollment target
Study Summary
The purpose of this study is to learn about the effect of different vaginal cuff closure techniques on pelvic support after laparoscopic hysterectomy and robotic assisted laparoscopic hysterectomy for benign gynecologic conditions.
Primary Outcome
The Pelvic Organ Prolapse - Quantification system is a validated way to measure pelvic organ prolapse. The investigators will measure this post op at 6-8 weeks to see if prolapse is better using one method vs the other.
Interventions
- PROCEDURE Laparoscopic - Vaginal Cuff Closure
- PROCEDURE Vaginal- Vaginal Cuff Closure
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 58 participants |
| Start Date | 2017-07-01 |
| Est. Completion | 2020-12-30 |
| Phase | NA |
Why NCT03753516 stopped before completion
NCT03753516 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 58 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 2 interventions - of which Laparoscopic - Vaginal Cuff Closure is the first listed.
NCT03753516 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03753516 about?
NCT03753516 is a clinical study titled "Pelvic Floor Support After Laparoscopic Hysterectomy for Benign Conditions: A Randomized Controlled Trial Comparing Vaginal Cuff Closure Techniques". The purpose of this study is to learn about the effect of different vaginal cuff closure techniques on pelvic support after laparoscopic hysterectomy and robotic assisted laparoscopic hysterectomy for benign gynecologic conditions.
What is the current status of trial NCT03753516?
This trial is currently terminated. It is a NA study. The enrollment target is 58 participants. The study started on 2017-07-01. Estimated completion is 2020-12-30.
What interventions are being tested in trial NCT03753516?
The interventions under investigation include: Laparoscopic - Vaginal Cuff Closure (PROCEDURE), Vaginal- Vaginal Cuff Closure (PROCEDURE).
Who is sponsoring clinical trial NCT03753516?
This trial is sponsored by Walter Reed National Military Medical Center, which has 48 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03753516's enrollment target sits among peer trials
58 1256th of 2000 higher than 740 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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