← Eichor
Study identifier: NCT04597372 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Impact of Tamsulosin on Post-Operative Urinary Retention Following Pelvic Reconstructive Surgery

Condition: Urinary Retention Postoperative  ·  Sponsor: Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)

PhasePhase 2
Planned participants154
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersYes

About this study

The objective of the study is to determine the effectiveness of postoperative Tamsulosin in reducing the duration of acute postoperative urinary retention (POUR) following pelvic reconstructive surgery through a double blind, randomized placebo-controlled trial.

This description comes directly from the study's public registry record.

Talk to the study team

Lindsay Turner  ·  (412)-330-4567  ·  lindsay.turner@AHN.ORG

AHN Clinical Trials Contact  ·  (412)-330-4567  ·  clinicaltrials@ahn.org

Always discuss trial participation with your own doctor first.

Locations (1)

West Penn HospitalPittsburgh, Pennsylvania, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT04597372