CompletedNot Applicable

Evaluation of a Novel Sutureless Drain Securement Device

United States22 participantsStarted 2022-03-07

Plain-language summary

The purpose of this study is to evaluate an investigational sutureless drain securement device (K-Lock) and compare this device to standard drain securement.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Age 18 or older * Patient of the Department of Plastic and Reconstructive Surgery * Able to sign English language Consent form * Undergoing any of the following procedures requiring placement of 2 or more drains (preferably bilateral) including: Breast reconstruction, Bilateral Breast Reduction, Abdominoplasty, Body Contour surgery (e.g. panniculectomy, brachiplasty, thighplasty) Exclusion Criteria: * Patients with unilateral drain placement * Unable to sign English language consent form * Allergy to Tegaderm Dressing

What they're measuring

Time it Takes to Secure and Dress Each Drain in Totality

Timeframe: Day of Surgery

Trial details

NCT IDNCT05251753

SponsorWake Forest University Health Sciences

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-03-06

Results submitted2025-03-07

View on ClinicalTrials.gov More Skin Injury trials