A Self-Controlled Clinical Study of Fast-Absorbable Versus Slow-Absorbable Sutures Applied in Ultra Tension-Reducing Suture Technique

Recruiting N/A Interventional Study
Ultra Tension-Reducing Suture Technique
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
20 (estimated)
Sponsor
Zhenzhen Zhang · Other
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About This Trial
Hypertrophic scar formation after wound healing remains a clinical challenge in plastic surgery. Ultra Tension-Reducing Suture Technique is currently the primary surgical option for preventing and reducing hypertrophic scarring.An ideal tension-relieving effect requires sustained support for 3 months postoperatively to align with the natural recovery cycle of skin tissue tensile strength. Studies …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Incision length ≥ 5 cm; 2. Clean, non-infected surgical wounds; 3. Ability to provide written informed consent voluntarily; 4. Scheduled for dermatologic surgery with intended linear wound closure; 5. Able to complete required postoperative follow-up; 6. No restriction on sur…
Contacts

Zhenzhen Zhang, MM

+86 18153957828

18153957828@163.com

CONTACT

Yonghong Qin, MD

+86 18919146244

1070936165@qq.com

CONTACT