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Comparing Tissue Adhesives in Port Site Closure

NCT05492721 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 180

Last updated 2026-02-09

No results posted yet for this study

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.

Conditions

  • Dermatitis, Contact

Interventions

DEVICE

2-Octylcyanoacrylate

Incisions on left will have one glue and on right will have the other glue

DEVICE

N-butyl-2-cyanoacrylate

Incisions on left will have one glue and on right will have the other glue

Sponsors & Collaborators

  • The University of Texas Health Science Center, Houston

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-06-29
Primary Completion
2025-06-23
Completion
2025-06-23
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05492721 on ClinicalTrials.gov