Comparing Tissue Adhesives in Port Site Closure

Completed · Phase 3

Conditions studied: Dermatitis, Contact

In brief

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.

Key facts

Study ID

NCT05492721

Run by

The University of Texas Health Science Center, Houston

People needed

180

Starts

2022-06-29

Expected to finish

2025-06-23

Last updated by the study team

2026-06-26

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 18 or older
• undergoing an elective laparoscopic or robotic abdominal surgery

You may not qualify if…

• 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.

Where it is running

• Memorial Hermann — Houston, Texas, United States

Full record on ClinicalTrials.gov

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