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NCT07217613 · ClinicalTrials.gov registry record · NA
Prospective Evaluation of Silk Fibroin Incision Dressings in ACL Reconstruction
A NA study, sponsored by NYU Langone Health.
- Recruiting
- Registry status
- NA
- Development phase
- 100
- Enrollment target
NCT07217613: Recruiting NA study, sponsored by NYU Langone Health.
NCT07217613 is a NA study that is actively recruiting participants, run by NYU Langone Health. The registered enrollment target is 100 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07217613, a NA study, is actively recruiting participants, sponsored by NYU Langone Health.
- RECRUITING
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
Study 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.
Primary Outcome
Incidence of allergic contact dermatitis, blistering, erythema, or other incision-related complications, assessed by the clinical team.
Interventions
- DEVICE silk fibroin-based incision dressing
- DEVICE cyanoacrylate-based closure system
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2025-10-14 |
| Est. Completion | 2026-07 |
| Phase | NA |
What NCT07217613 shows while recruiting
NCT07217613 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (93% lower).
The record links to 0 conditions, and to 2 interventions - of which silk fibroin-based incision dressing is the first listed.
NCT07217613 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT07217613 about?
NCT07217613 is a clinical study titled "Prospective Evaluation of Silk Fibroin Incision Dressings in ACL Reconstruction". 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.
What is the current status of trial NCT07217613?
This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2025-10-14. Estimated completion is 2026-07.
What interventions are being tested in trial NCT07217613?
The interventions under investigation include: silk fibroin-based incision dressing (DEVICE), cyanoacrylate-based closure system (DEVICE).
Who is sponsoring clinical trial NCT07217613?
This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT07217613's enrollment target sits among peer trials
100 840th of 2000 higher than 1,081 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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