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Cosmetic Outcomes of Absorbable Versus Non-absorbable Sutures in Pediatric Facial Lacerations (Catgut)

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Temple University

Status

Completed

Conditions

Lacerations
Wounds

Treatments

Other: Arm 2: Absorbable sutures
Other: Arm 1: non-absorbable sutures

Study type

Interventional

Funder types

Other

Identifiers

NCT00681070
11020-2
11020 (Registry Identifier)

Details and patient eligibility

About

Our research hypothesis in this study is that there is no difference in long-term cosmetic outcomes between absorbable sutures and non-absorbable sutures in the repair of pediatric facial lacerations.

Full description

The standard method of repair for facial lacerations is to close such wounds with non-absorbable sutures. Recently, topical skin adhesives such as n-butyl-2-cyanoacrylate and 2-octyl cyanoacrylate have been used more frequently as these have been shown to be a faster and less painful way to close superficial facial lacerations. However, lacerations that are deeper, gaping or occurring along lines of excessive tension, such as the chin, still need sutures for repair. Non-absorbable sutures have to be taken out at 4-7 days. This involves another physician visit, parental absence from work, and children who need to be taken out of school or daycare for a simple suture removal.

In Part Iof the study, we were able to demonstrate non-inferiority of absorbable sutures to nylon sutures. However, we purposely removed all remaining absorbable sutures on the 5-7 day follow-up visit. In Part II, we will allow the absorbable sutures to dissolve on their own. We will again assess long term cosmetic outcomes, as well parental satisfaction, and short and long-term complication rates at 3 months.

Enrollment

74 patients

Sex

All

Ages

1 to 18 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Clean. minimally contaminated facial lacerations, between 1-5 cms long, less than 8 hours old, not caused by animal bites, not needing plastic surgery repair

Exclusion criteria

  • Pregnancy
  • Bleeding
  • Renal
  • Endocrine problems
  • Dirty wounds
  • Irregular wounds

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

74 participants in 2 patient groups

Arm1: Non-absorbable sutures
Active Comparator group
Description:
use of non-absorbable sutures in facial laceration in this arm
Treatment:
Other: Arm 1: non-absorbable sutures
Arm 2: Absorbable sutures
Active Comparator group
Description:
use of absorbable sutures in this arm
Treatment:
Other: Arm 2: Absorbable sutures

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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