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Pre-operative Polyethylene Glycol 3350 for Minimally Invasive Urogynecologic Surgery

StatusCompleted
PhasePhase 4
Started
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Record History

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  1. Results posted: Sep 22, 2026
    • Eligibility criteria expanded, about 12 words
    • Secondary endpoints revised (5)
    • Study description expanded, about 2 words
  2. Enrollment target: 74 to 72
    • Secondary endpoints revised (5)
    v10
  3. Trial status: Recruiting to Completed
    • Primary and study completion dates changed from estimate of Apr 30, 2026 to Mar 13, 2026
    • Site details revised
    v9
  4. Primary and study completion dates: Dec 1, 2025 to Apr 30, 2026v8
  5. Primary and study completion dates: Jul 1, 2025 to Dec 1, 2025v7
Show 5 earlier versionsHide 5 earlier versions
  1. Primary and study completion dates: Feb 2025 to Jul 1, 2025v6
  2. Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Aug 2024 to Jun 5, 2024
    • Site details revised
    v5
  3. Study sites: 0 to 1v4
  4. Start date: Feb 2024 to Aug 2024v3
  5. Study completion date: Jun 2025 to Feb 2025
    • Secondary endpoints: 4 to 5
    v2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this clinical trial is to test the use of a laxative before surgery in women having surgery to fix pelvic prolapse that do not have constipation. The main question it aims to answer is: Does use of a laxative before surgery lessen the discomfort of bowel movements after surgery? Participants will be asked to complete questionnaires before and after surgery. Researchers will compare using the laxative before and after surgery versus only after surgery to see if there is less discomfort with bowel movements after surgery.
Trial Details
NCT Number NCT06159777
Lead Sponsor University Hospitals Cleveland Medical Center
Conditions
(from sponsor)		 Constipation, Surgical Procedure, Unspecified, Prolapse; Female
Related terms Constipation, Prolapse
Enrollment 72 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov