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RECRUITING
NCT07217613
NA

Prospective Evaluation of Silk Fibroin Incision Dressings in ACL Reconstruction

Sponsor: NYU Langone Health

View on ClinicalTrials.gov

Summary

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.

Official title: Prospective Evaluation of Silk Fibroin Versus 2-Octyl Cyanoacrylate Incision Dressings Following ACL Reconstruction

Key Details

Gender

All

Age Range

14 Years - 60 Years

Study Type

INTERVENTIONAL

Enrollment

100

Start Date

2025-10-14

Completion Date

2026-07

Last Updated

2026-05-08

Healthy Volunteers

No

Interventions

DEVICE

silk fibroin-based incision dressing

Applied sterile, hydrophobic, hypoallergenic dressing remains in place for 14-21 days, unless removal is clinically indicated (e.g., saturation, detachment, suspected allergic contact dermatitis, or at provider discretion).

DEVICE

cyanoacrylate-based closure system

Applied per standard NYU practice; dressing remains in place per routine protocol.

Locations (1)

NYU Langone Health

New York, New York, United States