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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.

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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

FieldValue
Enrollment Target 4 participants
Start Date 2013-08
Est. Completion 2014-11
Phase Phase 4

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.