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Bowel Preparation for Colonoscopy Among Individuals With Crohn's and Ulcerative Colitis Disease.

StatusRecruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated January 8, 2025 (before its estimated December 2025 completion). Its status may not reflect the trial's current state.

Record History

  1. Notable Trial status: Not Yet Recruiting to Recruiting
    • Primary completion date: Mar 2025 to Dec 2025
    • Study completion date: Jun 2025 to May 2026
    • Start date changed from estimate of May 2024 to Jul 4, 2024
    v3
  2. Notable Start date: Mar 2024 to May 2024v2
  3. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 purpose of this study is to compare how effective and how tolerable two different bowel preparation laxatives are for colonoscopy. The aim is to compare oral sulfate solution (OSS) to another laxative called 2L polyethylene glycol (PEG) solution to see which is more effective and more tolerable by individuals with IBD (Crohn's disease or Ulcerative colitis).
Trial Details
NCT Number NCT06298461
Lead Sponsor University of Manitoba
Collaborators: Canadian IBD Research Consortium (CIRC)
Conditions
(from sponsor)
Crohn Disease, Ulcerative Colitis
Related terms Colitis, Ulcerative, Crohn Disease
Enrollment 418 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov