Disposable noninvasive skin closure to help healing and reduce scarring after plastic surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Adults undergoing plastic surgery with incisions longer than 2 cm on the face, neck, trunk, or limbs will be enrolled. Each incision is split, with the device applied to one half and standard care on the other half. Wound healing and scar appearance are evaluated at 1, 3, and 6 months by blinded plastic surgeons using standardized scar-rating tools. The study aims to determine the device’s safety and whether it improves healing and reduces scar formation compared with conventional care.

Why it matters

Who can join: the full rules

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

Where it's running

• Peking University Third Hospital
  Beijing, Beijing Municipality, China Recruiting

Study contacts

• Principal investigator: Yimou Sun, M.D. — Peking University Third Hospital
• Study coordinator: Yimou Sun, M.D.
• Email: sym316@126.com
• Phone: +86 13811625471

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.