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NCT03835351 · ClinicalTrials.gov registry record · NA
Urinary Retention After Laparoscopic Inguinal Hernia Repair: Comparing the Use of the Intraoperative Urinary Catheter
A NA study, sponsored by The Cleveland Clinic.
- Completed
- Registry status
- NA
- Development phase
- 491
- Enrollment target
NCT03835351: Completed NA study, sponsored by The Cleveland Clinic.
NCT03835351 is a NA study that has completed, run by The Cleveland Clinic. The registered enrollment target is 491 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (65% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03835351, a NA study, has completed, sponsored by The Cleveland Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 491 participants
- Enrollment target
Study Summary
This will be a randomized controlled study which will compare the rate of post-operative urinary retention after laparoscopic inguinal hernia repair between patients who receive an intra-operative urinary catheter and those who do not. The primary aim of the study is to determine if the use of intra-operative urinary catheter reduces the incidence of post-operative urinary retention after laparoscopic inguinal hernia repair. Specific patient inclusion criteria include all patients aged 18 years or older presenting for an elective unilateral or bilateral inguinal hernia repair, who are able to tolerate general anesthesia and are considered eligible to have a hernia repair through a laparoscopic approach.
Primary Outcome
The rate of postoperative urinary retention requiring insertion of a urinary catheter
Interventions
- DEVICE Urinary Catheter
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 491 participants |
| Start Date | 2019-03-07 |
| Est. Completion | 2021-04-15 |
| Phase | NA |
What the finished NCT03835351 record still lists
NCT03835351 is an interventional study that assigns participants to a tested intervention. The registered 491 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 (65% lower).
The record links to 0 conditions, and to 1 intervention - of which Urinary Catheter is the first listed.
NCT03835351 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03835351 about?
NCT03835351 is a clinical study titled "Urinary Retention After Laparoscopic Inguinal Hernia Repair: Comparing the Use of the Intraoperative Urinary Catheter". This will be a randomized controlled study which will compare the rate of post-operative urinary retention after laparoscopic inguinal hernia repair between patients who receive an intra-operative urinary catheter and those who do not. The primary aim of the study is to determine if the use of intra...
What is the current status of trial NCT03835351?
This trial is currently completed. It is a NA study. The enrollment target is 491 participants. The study started on 2019-03-07. Estimated completion is 2021-04-15.
What interventions are being tested in trial NCT03835351?
The interventions under investigation include: Urinary Catheter (DEVICE).
Who is sponsoring clinical trial NCT03835351?
This trial is sponsored by The Cleveland Clinic, which has 688 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03835351's enrollment target sits among peer trials
491 215th of 2000 higher than 1,786 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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