CompletedPhase 3

Comparing Tissue Adhesives in Port Site Closure

United States180 participantsStarted 2022-06-29

Plain-language summary

This is a multi-center randomized controlled trial to evaluate two different methods of reinforcing surgical port site closure: 2-Octylcyanoacrylate and n-butyl-2-cyanoacrylate.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 18 or older * undergoing an elective laparoscopic or robotic abdominal surgery Exclusion Criteria: * Patients unlikely to follow-up (live out of state, unable to be reached by phone or email) * Patients with a known allergy to 2-Octylcyanoacrylate or N-butyl-2-cyanoacrylate.

What they're measuring

proportion of patients who develop contact dermatitis

Timeframe: 6 weeks

Trial details

NCT IDNCT05492721

SponsorThe University of Texas Health Science Center, Houston

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-06-23

View on ClinicalTrials.gov More Dermatitis, Contact trials