Clinical Trials Directory

Trials / Completed

CompletedNCT02958878

Preoperative Administration of Tamsulosin for Prevention of Post Operative Urinary Retention in Males Undergoing Elective Inguinal Hernia Repair

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
210 (actual)
Sponsor
Ascension Health · Industry
Sex
Male
Age
30 Years
Healthy volunteers
Accepted

Summary

Double blinded, randomized controlled prospective study looking at 2 preoperative doses of Tamsulosin an alpha-adrenergic blocker in preventing post-operative urinary retention. A previous study was conducted called "Effectiveness of tamsulosin inprevention of postoperative urinary retention: a randomized double-blind-placebo controlled study" This study involved a tertiary care center involving mostly urological surgical procedures. We look to specifically look at inguinal hernia surgeries in males. The aim of this study is to compare the prophylactic effect of tamsulosin with placebo on postoperative urinary retention. The drug is FDA approved for benign prostatic hypertrophy and urinary retention. It is on formulary at Genesys. Currently there is no standard procedure of prophylactic tamsulosin for urinary retention. Most often post operative patients are given tamsulosin to augment smooth muscle relaxation and spontaneous voiding if the patient is having urinary retention post operatively. We often straight catheterize patients once and start tamsulosin with the goal of avoiding urinary retention and future straight catheterizations or placement of foley catheters

Conditions

Interventions

TypeNameDescription
DRUGTamsulosin
DRUGPlacebo Oral Capsule

Timeline

Start date
2017-01-03
Primary completion
2018-11-30
Completion
2018-11-30
First posted
2016-11-08
Last updated
2019-07-30

Source: ClinicalTrials.gov record NCT02958878. Inclusion in this directory is not an endorsement.