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Post Operative Skin Approximation With Cyanoacrylate Based Wound Closure Adhesives

NCT07613892 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2026-05-29

No results posted yet for this study

Summary

surgical adhesive systems are used to close surgical cuts and simple skin wounds. This system is a non-invasive option, meaning it can be used instead of stitches or staples. Because these products do not require stitching deep into the skin, they can reduce the time it takes to close a wound and may reduce stress or damage to the skin edges.

Conditions

  • Wound Closure
  • Dehisced Surgical Wounds

Interventions

DEVICE

Evaluating wound closure products to close larger surgical site incisions

Participants receive surgical incision closure using either OptiClose or Dermabond, selected through randomization based on incision characteristics. Incisions requiring mesh support (\>20 cm) are closed with adhesive plus mesh using one of the assigned products.

DEVICE

Evaluating wound closure products to close smaller surgical site incisions

Participants receive surgical incision closure using either OptiClose or Dermabond, selected through randomization based on incision characteristics. Incisions not requiring mesh (≤19 cm) are closed using cyanoacrylate-based adhesive alone. Product assignment is randomized within each incision category.

Sponsors & Collaborators

  • Medline Industries

    lead INDUSTRY

Principal Investigators

  • Scott Dupar, Physician - Doctor of Medicine · Nadora Healthcare

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-04-02
Primary Completion
2026-03-18
Completion
2026-03-18
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 NCT07613892 on ClinicalTrials.gov