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NCT03685565 | COMPLETED | Facial Laceration


Facial Lacerations Repaired With Dermabond Compared With Dermabond With Underlying Steristrips in Pediatric Patients
Sponsor:

University of Texas at Austin

Information provided by (Responsible Party):

Erin d munns

Brief Summary:

The purpose of the study is to compare cosmetic outcomes of simple facial lacerations in children repaired with Dermabond (skin glue) compared with Dermabond (skin glue) with underlying steristrips (skin adhesive strips).

Condition or disease

Facial Laceration

Intervention/treatment

Dermabond and steristrips

Dermabond

Phase

NA

Study Type : INTERVENTIONAL
Estimated Enrollment : 120 participants
Masking : DOUBLE
Primary Purpose : TREATMENT
Official Title : Cosmetic Outcomes of Simple Facial Lacerations Repaired With Dermabond Compared With Dermabond With Underlying Steristrips: A Randomized Controlled Trial
Actual Study Start Date : 2018-09-15
Estimated Primary Completion Date : 2020-01-15
Estimated Study Completion Date : 2020-01-15

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: to 17 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Age ≤17 years old
  • * Presents with simple, linear facial laceration requiring repair
  • * English or Spanish speaking parents or guardians
Exclusion Criteria
  • * Laceration to lips, nose, ear, eyelids, eyebrows
  • * Laceration requiring multi-layer closure
  • * Laceration requiring sub-specialty care
  • * Laceration that has previously been repaired
  • * Animal/human bites
  • * Lacerations \>5cm in length
  • * Allergy to adhesive

Facial Lacerations Repaired With Dermabond Compared With Dermabond With Underlying Steristrips in Pediatric Patients

Location Details

NCT03685565


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Locations


Not yet recruiting

United States, Texas

Dell Children's Hospital

Austin, Texas, United States, 78723

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