Actively Recruiting

Phase 3
Age: 18Years +
FEMALE
NCT06843538

Peri-operative Tamsulosin and Impact on Voiding Trial After Same-day Urogynecology Surgery

Led by TriHealth Inc. · Updated on 2025-02-25

166

Participants Needed

1

Research Sites

69 weeks

Total Duration

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AI-Summary

What this Trial Is About

The purpose of this research study is to determine if taking tamsulosin preoperatively decreases your chances of being discharged after surgery with a Foley catheter (flexible tube that drains urine from the bladder into a collection bag).

CONDITIONS

Official Title

Peri-operative Tamsulosin and Impact on Voiding Trial After Same-day Urogynecology Surgery

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients undergoing any pelvic organ prolapse repair or incontinence surgery
Not Eligible

You will not qualify if you...

  • Surgery involving a non-urogynecologist
  • Current use of alpha blocker medication
  • Baseline low blood pressure (hypotension)
  • History of fainting (syncope)
  • Postural orthostatic tachycardia syndrome (POTS)
  • Non-English speaking without available interpreter for Spanish
  • Cognitive impairment preventing proper consent
  • Any medical reason preventing tamsulosin use
  • History of urinary retention needing catheterization
  • Pregnancy
  • Intraoperative complications requiring catheter use or voiding trial no longer indicated

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

TriHealth

Cincinnati, Ohio, United States, 45220

Actively Recruiting

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Research Team

G

Gisele C Moran, MD, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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