Prospective Evaluation of Silk Fibroin Incision Dressings in ACL Reconstruction
Recruiting
N/A
Interventional Study
Anterior Cruciate Ligament Reconstruction
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 14 – 60
- Sex
- Any
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 100 (estimated)
- Sponsor
- NYU Langone Health · Other
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About This Trial
The purpose of this study is to compare the incidence of early postoperative skin complications including allergic contact dermatitis, blistering, and erythema between silk fibroin incision dressings and cyanoacrylate closure in patients undergoing anterior cruciate ligament reconstruction.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age 14 to 60 years
* Scheduled for primary or revision ACL reconstruction (ACLR)
* Able and willing to provide informed consent (≥18 years) or assent with parental/guardian permission (ages 14-17)
* Able and willing to comply with all study-related procedures and follow-up vis…
Contacts