Status:
COMPLETED
Evaluation of a Novel Sutureless Drain Securement Device
Lead Sponsor:
Wake Forest University Health Sciences
Conditions:
Skin Injury
Eligibility:
All Genders
18+ years
Phase:
NA
Brief 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.
Detailed Description
This study will evaluate the feasibility, safety and efficacy of a novel sutureless drain securement device (K-Lock) via direct comparison to suture-based techniques. In this study the sutureless drai...
Eligibility Criteria
Inclusion
- 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
- Patients with unilateral drain placement
- Unable to sign English language consent form
- Allergy to Tegaderm Dressing
Key Trial Info
Start Date :
March 7 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 6 2025
Estimated Enrollment :
22 Patients enrolled
Trial Details
Trial ID
NCT05251753
Start Date
March 7 2022
End Date
March 6 2025
Last Update
May 20 2025
Active Locations (1)
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1
Atrium Health Wake Forest Baptist
Winston-Salem, North Carolina, United States, 27157