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Ostomy Primary Closure With 0.1% Betaine/Polyhexanide Wound Irrigation Compared to Pursestring Closure

RecruitingPhase 4Ages 18 Years - anyAllUniversity of Nevada, Las Vegas
NCT06309368 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The goal of this clinical trial is to compare two types of closure in patients with ostomies that are ready for closure. The main questions it aims to answer are: 1. Surgical site infection rates 2. Patient quality of life 3. Time to wound healing Participants will undergo either complete ostomy wound closure after washing out the wound with Prontosan, or their ostomy wound will be closed using the Pursestring method, where the wound will be left partially open and allowed to heal from the inside out. Researchers will compare these two groups' outcomes (questions to be answered) as listed above.

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📋 Eligibility rules (as published)
Inclusion Criteria: * All patients 18 years or older with an diverting loop ileostomy reversal indication will be enrolled * Signed consent Exclusion Criteria: * Under 18 years old, unable to provide consent, has a parastomal hernia requiring mesh repair, or has an end ileostomy
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What it tests

  • Primary Ostomy Closure with 0.1% Betaine/0.1% Polyhexanide Wound Irrigation
  • Pursestring Closure
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Where

1 site
University Medical Center
Las Vegas, United States
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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