Clinical Trials Directory

Trials / Unknown

UnknownNCT03027115

Hernia Surgery Urinary Retention

Post-operative Urinary Retention: A Prospective Randomized Study Identifying Patients at Risk and Reducing the Incidence Using Tamsulosin Pretreatment

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
140 (estimated)
Sponsor
Memorial Health University Medical Center · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

Investigating whether pre-operative treatment with a selective alpha1-adrenoceptor antagonist affects the likelihood of male patients developing post-operative urinary retention following hernia repair.

Detailed description

The purpose of this study will be to investigate whether pre-operative treatment with a selective alpha1-adrenoceptor antagonist affects the likelihood of male patients developing post-operative urinary retention following hernia repair surgery. It is also of interest to determine whether or not a well-known urological screening tool, the IPSS, can identify patients at risk for urinary retention following elective laparoscopic or open hernia repair surgery. We will investigate if it is possible to pre-treat patients with a selective alpha1-adrenoceptor antagonist which we think can reduce the incidence of post-operative urinary retention and the associated adverse consequences, especially in those patients at higher risk.

Conditions

Interventions

TypeNameDescription
DRUGTamsulosinTamsulosin treatment for 7 days pre-operatively

Timeline

Start date
2017-01-13
Primary completion
2020-01-13
Completion
2020-01-27
First posted
2017-01-20
Last updated
2018-03-23

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03027115. Inclusion in this directory is not an endorsement.