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Patient Reported Experiences and Outcomes Associated with Standard C-Section Wound Closure Versus STRATAFIX/DERMABOND PRINEO Wound Closure (CS-PREO)

RecruitingNAAges 18 Years - anyFemaleNorth York General Hospital
NCT06614829 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The aim of the study is to compare outcomes between patients receiving standard C-section wound closure compared to a wound closure bundle that includes Stratafix sutures and Dermabond PRINEO.

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📋 Eligibility rules (as published)
Inclusion Criteria: 1. Patient must be 18 years of age or older at time of recruitment 2. Patients opting for a planned (elective) C-Section (13-36 weeks gestation) will be eligible to consent. 3. Patients must have internet access and/or a smartphone in order to access the digital platform to complete the study questionnaires 4. Patients must speak and write in English as study questionnaires will only be provided in English 5. Patients must have coverage from the Ontario Health Insurance Plan (OHIP) Exclusion Criteria: 1. Patients assessed by the participating surgeon with any conditions that may compromise their: * Ability to consent or use the virtual care platform (e.g., patients with intellectual disabilities) * Expectation of significant maternal complications that may affect the surgery 2. Patients who enroll in the study but have an unplanned emergency C-section
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What it tests

  • Stratafix Suture
  • DERMABOND PRINEO
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Where

1 site
North York General Hospital
North York, Canada
🤝 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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