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

RecruitingNAAges 20 Years - 50 YearsAllPeking University Third Hospital
NCT07849010 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Adults aged 20 to 50 years undergoing plastic surgery * Surgical incision located on the cheek, neck, trunk, or limbs, excluding the hands and feet * Surgical incision longer than 2 cm * Willing and able to provide written informed consent Exclusion Criteria: * History of abnormal scar formation or keloids * Autoimmune disease * Surgical wound infection * Use of any scar treatment or wound treatment other than the study device during the study period
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What it tests

  • Disposable Noninvasive Skin Closure Device (Shanghai Zhizhong Medical Technology Co., Ltd. Catalog No.: 240430PFF)
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Where

1 site
Peking University Third Hospital
Beijing, China
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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