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Disposable Noninvasive Skin Closure for Promoting Postoperative Wound Healing and Preventing Surgical Skin Scarring

StatusRecruiting
PhaseNot applicable
Started2026-10-01
View on ClinicalTrials.gov ↗
The purpose of this study is to evaluate the efficacy and safety of a disposable noninvasive skin closure device in promoting postoperative wound healing and reducing surgical scar formation. Participants will receive the device on one half of the surgical incision, with the other half serving as a control. Wound healing and scar appearance will be assessed during follow-up visits after surgery.
Trial Details
NCT Number NCT07849010
Lead Sponsor Peking University Third Hospital
Conditions Scar
Enrollment 25 participants
Start Date 2026-10-01
Primary Completion 2027-06-30 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-09-30