Status:
TERMINATED
Cosmetic Outcome Study of Lid Laceration Repair With Suture Versus Tissue Adhesive
Lead Sponsor:
The University of Texas Health Science Center, Houston
Conditions:
Eyelid Laceration
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
This project is a randomized, controlled trial investigating wound cosmetic appearance after repair of traumatic lid lacerations with three different approaches to skin closure: absorbable sutures, no...
Detailed Description
This project is a randomized, controlled trial investigating the cosmetic appearance after repair of traumatic lid lacerations with three different approaches to skin closure: absorbable sutures (surg...
Eligibility Criteria
Inclusion
- 18 years of age or older.
- Any laceration caused by trauma and involving the skin of the upper and/or lower eyelid.
- Must be able to understand and sign an informed consent when applicable and Health Insurance Portability and Accountability Act(HIPAA) form that has been approved by an Institutional Review Board (IRB) or follow standard informed consent procedure of the IRB
Exclusion
- Eyelid lacerations that include avulsion or missing eyelid tissue
- Patients with known hypersensitivity to octyl-2-cyanoacrylate or previous poor reaction to octyl-2-cyanoacrylate
- Eyelid lacerations resulting in necrosis or ischemia of tissue prior to repair
- Patients who demonstrate intoxication or mental status changes that would make them unfit to provide informed consent for repair
Key Trial Info
Start Date :
August 1 2013
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 2014
Estimated Enrollment :
4 Patients enrolled
Trial Details
Trial ID
NCT01918059
Start Date
August 1 2013
End Date
November 1 2014
Last Update
December 3 2014
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Memorial Hermann Hospital - Texas Medical Center
Houston, Texas, United States, 77030