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NCT01918059 · ClinicalTrials.gov registry record · Phase 4
Cosmetic Outcome Study of Lid Laceration Repair With Suture Versus Tissue Adhesive
A Phase 4 study, sponsored by The University of Texas Health Science Center, Houston.
- Terminated
- Registry status
- Phase 4
- Development phase
- 4
- Enrollment target
NCT01918059 is a Phase 4 study that was terminated before completion, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 4 participants.
The verdict
NCT01918059, a Phase 4 study, was terminated before completion, sponsored by The University of Texas Health Science Center, Houston.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 4 participants
- Enrollment target
Study 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, non-absorbable sutures, and tissue adhesive. Photographs will be taken at two intervals after repair and later blindly assessed using standard cosmetic assessment scales. The investigators hypothesize that cosmetic wound outcome will be equivalent in across all three treatment arms.
Interventions
- PROCEDURE Tissue Adhesive skin closure
- PROCEDURE Absorbable suture skin closure
- PROCEDURE Non-absorbable suture skin closure
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 4 participants |
| Start Date | 2013-08 |
| Est. Completion | 2014-11 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01918059
The ClinicalTrials.gov registry entry for NCT01918059 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 4 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Tissue Adhesive skin closure is the first listed.
NCT01918059 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01918059 about?
NCT01918059 is a clinical study titled "Cosmetic Outcome Study of Lid Laceration Repair With Suture Versus Tissue Adhesive". 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, non-absorbable sutures, and tissue adhesive. Photographs will be taken at two intervals after repair a...
What is the current status of trial NCT01918059?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 4 participants. The study started on 2013-08. Estimated completion is 2014-11.
What interventions are being tested in trial NCT01918059?
The interventions under investigation include: Tissue Adhesive skin closure (PROCEDURE), Absorbable suture skin closure (PROCEDURE), Non-absorbable suture skin closure (PROCEDURE).
Who is sponsoring clinical trial NCT01918059?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
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