Clinical Trials Logo
  1. Home
  2. Postoperative Urinary Retention
  3. NCT05276804

The POUR (Postoperative Urinary Retention) Study — POUR  

Postoperative Urinary Retention Clinical Trial

Official title:
The POUR Study: Effects of Neuromuscular Reversal Agents on Postoperative Urinary Retention (POUR) Following Laparoscopic Inguinal Hernia Repair

Clinical Trial Summary

The primary aim of this study will be to compare the rate of postoperative urinary retention between patients receiving Sugammadex and those receiving traditional reversal agents

Clinical Trial Description

Postoperative urinary retention following laparoscopic inguinal hernia repair occurs in approximately one out of ten patients. The more rapid reversal of neuromuscular blockade with Sugammadex has empirically been associated with low rates of postoperative urinary retention. In this study, patients will receive Sugammadex following laparoscopic inguinal hernia repair and then be retrospectively matched against a group of patients who did not receive Sugammadex. The primary aim of this study will be to compare the rate of postoperative urinary retention between patients receiving Sugammadex and those receiving traditional reversal agents (e.g. neostigmine which has a retention rate of 5-11%). We will also examine difference in cost and quality of life between the two groups. Our hypothesis is that the use of Sugammadex will decrease rate of postoperative urinary retention, decrease associated cost, such as need for admission, and not negatively impact quality of life. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05276804
Study type Interventional
Source Wake Forest University Health Sciences
Contact Brant T Heniford, MD
Phone 704-355-3168
Email Todd.Heniford@AtriumHealth.org
Status Recruiting
Phase Phase 3
Start date April 13, 2022
Completion date June 2025
View Details
See also
  Status Clinical Trial Phase
Completed NCT03341819 - Comparative Study Between Retained and Non-retained Urinary Catheter in Total Knee Arthorplasty With Epidural Anesthesia N/A
Completed NCT05428020 - RCT Foley Catheter Study for Elective TJA N/A
Completed NCT05969145 - The Effect of Hot-Cold Application to the Bladder After Orthopedic Surgery on Postoperative Urinary Retention N/A
Completed NCT02133768 - Routine Bladder Catheterisation Through Fast-track Hip and Knee Replacement - What Are the Consequences? N/A
Recruiting NCT01568918 - Use of Tamsulosin to Reduce the Incidence and Duration of Postoperative Urinary Retention Following Spine Surgery Phase 3
Completed NCT05898919 - Acupuncture for Postoperative Urinary Retention After Hemorrhoidectomy: a Randomized Controlled Trial Phase 2
Completed NCT02958878 - Preoperative Administration of Tamsulosin for Prevention of Post Operative Urinary Retention in Males Undergoing Elective Inguinal Hernia Repair Phase 4
Completed NCT02996968 - Self-discontinuation of a Transurethral Catheter N/A
Withdrawn NCT03937531 - Void Trials After Two Voiding Trials (TVT) N/A
Recruiting NCT05664633 - The Role of Sugammadex in Posotoperative Urinary Retention in Patients Undergoing Pelvic Floor Reconstructive Procedures Phase 1/Phase 2
Terminated NCT02518971 - Trial of Prophylactic Tamsulosin for Postoperative Urinary Retention in Primary Total Hip and Knee Arthroplasty Patients Phase 3
Not yet recruiting NCT06258785 - Effect of Tizanidine on Postoperative Urinary Retention After Sacrospinous Suspension Phase 3