3M™ Topical Tissue Adhesive Versus Commercially Available Tissue Adhesive for the Closure of Lacerations and Incisions
NCT06217081 · Status: TERMINATED · Type: INTERVENTIONAL · Enrollment: 78
Last updated 2026-07-27
Summary
The purpose of this study is to generate safety and performance data for 3M™ Topical Tissue Adhesive. Enrolled subjects with qualifying trauma lacerations or surgical incisions will be randomized to receive 3M™ Topical Tissue Adhesive or Histoacryl® Blue Topical Skin Adhesive with follow-up visits at 10 days and 30 days after application of tissue adhesive.
Conditions
- Trauma-related Wound
- Surgical Incision
- Surgical Wound
- Laceration
Interventions
- DEVICE
-
3M Topical Tissue Adhesive
Application of investigational topical tissue adhesive to trauma laceration or surgical incision.
- DEVICE
-
Histoacryl® Blue Topical Skin Adhesive
Application of control topical tissue adhesive to trauma laceration or surgical incision.
Sponsors & Collaborators
-
United States Department of Defense
collaborator FED -
The University of Texas Health Science Center at San Antonio
collaborator OTHER -
3M
collaborator INDUSTRY -
Solventum US LLC
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 22 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2024-10-28
- Primary Completion
- 2025-06-24
- Completion
- 2025-06-24
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