Actively Recruiting

Phase Not Applicable
Age: 18Years - 99Years
FEMALE
NCT07372547

Effect of Voiding Position (Standing in the Shower vs. Sitting) on Post-Void Residual Urine Volume (PVR) After Removal of Urinary Catheter in Women Following Benign Vaginal Gynecologic Surgery

Led by Assuta Ashdod Hospital · Updated on 2026-03-25

100

Participants Needed

2

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if voiding in a standing position in the shower, rather than sitting on a toilet, may reduce pain associated with the act of voiding, thereby facilitating micturition and decreasing both post-void residual volume and the risk of subsequent urinary retention in women that underwent benign vaginal surgeries.

CONDITIONS

Official Title

Effect of Voiding Position (Standing in the Shower vs. Sitting) on Post-Void Residual Urine Volume (PVR) After Removal of Urinary Catheter in Women Following Benign Vaginal Gynecologic Surgery

Who Can Participate

Age: 18Years - 99Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult women (≥18 years old)
  • Undergoing benign vaginal gynecologic surgery with urinary catheter during surgery
  • No bladder injury during surgery
  • Ability and willingness to consent
  • No neurological or urinary conditions affecting urination
  • No active urinary tract infection at catheter removal
Not Eligible

You will not qualify if you...

  • Bladder injury during surgery
  • Neurological disease affecting bladder function
  • Active urinary tract infection
  • Inability to urinate standing in shower or sitting (based on group assignment)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Assuta Ashdod Hospital

Ashdod, Israel

Not Yet Recruiting

2

Assuta Ashdod Medical Center

Ashdod, Israel

Actively Recruiting

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Research Team

E

Elad Preuss, M.D

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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