Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07174349

Uroselective Alpha-1-Antagonist to Reduce the Incidence and Duration of Postoperative Urinary Retention Following Spine Surgery

The Use of an Uroselective Alpha-1-antagonist to Reduce the Incidence and Duration of Postoperative Urinary Retention Following Spine Surgery

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
20 (estimated)
Sponsor
Mayo Clinic · Academic / Other
Sex
All
Age
35 Years
Healthy volunteers
Not accepted

Summary

The purpose of this research is to see if the use of tamsulosin can decrease both the incidence and duration of urinary retention, as well as hospital length of stay following spine surgery.

Detailed description

Postoperative urinary retention is a frequent complication of spinal surgeries and impacts a large portion of this population which results in increased morbidity as a result of increased number of catheterizations, urinary tract infections and prolonged hospital stays. With the addition of Tamsulosin, we would anticipate a reduction in the incidence and duration of postoperative urinary retention and therefore a reduction in morbidity related to treatment of urinary retention as well as shortened hospital stays.

Conditions

Interventions

TypeNameDescription
DRUGUroselective alpha-1-adrenergic receptor antagonistSubjects will receive Tamsulosin (0.4 mg daily) beginning 5 days prior to surgery and for the duration of the postoperative hospital stay (approximately 8-12 days)
OTHERPlaceboSubjects will receive placebo beginning 5 days prior to surgery and for the duration of the postoperative hospital stay (approximately 8-12 days)

Timeline

Start date
2026-04-10
Primary completion
2027-01-31
Completion
2028-12-31
First posted
2025-09-15
Last updated
2026-04-03

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07174349. Inclusion in this directory is not an endorsement.