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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 is a NA study that has completed, run by The Cleveland Clinic. The registered enrollment target is 491 participants.
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.
Interventions
- DEVICE Urinary Catheter
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 491 participants |
| Start Date | 2019-03-07 |
| Est. Completion | 2021-04-15 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03835351
The ClinicalTrials.gov registry entry for NCT03835351 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 491 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The Cleveland Clinic, which has 688 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Urinary Catheter is the first listed.
NCT03835351 reports 0 study locations.
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.
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