Recruiting

Suture Removal

Sponsor:

DermSurgery Associates

Code:

NCT05267002

Conditions

Suture; Complications, Mechanical

Scar

Surgery

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Interventions

Suture removal timing

Study Details

Brief summary:

Our goal is to compare the difference in surgical outcomes and patient satisfaction for surgical scars on the face between suture removal at 1 week versus 2 weeks.

There is variation in the timing at which Mohs surgeons remove sutures on the face. Some prefer 1 week, and others prefer 2 weeks. This has not been formally studied. It is possible the outcomes are the same between both groups, or that one has a better cosmetic outcome than the other.

Your skin cancer will be removed as usual. After this, your wound will be sutured in the usual fashion, except the top sutures will be divided into two separate halves. You will return at 1 week for one half of the top sutures to be removed, and at 2 weeks for the other half to be removed. Which half is removed first will be determined at random at your 1 week visit. At two months, you will return for standardized photographs which will be used by physicians to rate the cosmetic outcomes of the wound halves based on a standardized scale. Most likely, there will be no difference between the wound halves at 2 months and the study is complete. There is a small chance that there will be a cosmetic difference seen at 2 months, in which case you will return at 1 year for repeat standardized photographs and ratings. All data and photographs will be kept secure and any identifying information will be destroyed at the end of the study.

Conditions

Suture; Complications, Mechanical

Scar

Surgery

Study ID

NCT05267002

Start date

Feb 24, 2022

Status verified date

Feb, 2022

Completion date

May 24, 2023

Anticipated

Primary completion date

May 24, 2023

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Inclusion Criteria i. Adult patients >18 years ii. Undergoing Mohs surgery or excision with layered repair

1. intermediate or complex layered closures measuring 2.6-7.5 cm on the face (including the forehead, temples, nose, cheeks, chin)
2. Wound edges must be able to be approximated with subcutaneous sutures. iii. Ability to follow up at 1 week, 2 weeks, 2 months, and 1 year iv. Participants able to be enrolled at time of wound repair.

Exclusion criteria i. Facial defects involving the eyelid, mucosal lip, and ear ii. Pregnant or breastfeeding women iii. Children <18 years iv. Inability to comprehend English v. Inability to consent vi. Incarceration

Study Design

Enrollment

68 participants

Anticipated

Allocation

Randomized

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Suture removal at 1 week

Cutaneous nylon suture removal of half of the split-scar at one week.

experimental: Suture removal at 2 weeks

Cutaneous nylon suture removal of half of the split-scar at two weeks.

Interventions

Suture removal timing

Cutaneous nylon suture removal of each half of the split-scar at one and two weeks.

Primary outcome measure

  • Scar Cosmesis Assessment and Rating scale (SCAR) score [ Time Frame: 2months (and possibly one year, see protocol) ]

Central Contacts and Locations

Locations

DermSurgery Associates

Recruiting

Houston, Texas, United States, 77030

Contacts

More Information

Sponsor

DermSurgery Associates

Last update posted

Mar 4, 2022

Last verified

Feb, 2022

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by DermSurgery Associates on 2022-03-04.