Status:
RECRUITING
Evaluating the Effect of Surgical Drain Securement on Patient Quality of Life and Postoperative Drain-related Complications
Lead Sponsor:
Wake Forest University Health Sciences
Collaborating Sponsors:
University of Mississippi Medical Center
Conditions:
Surgical Drain
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The objective of this study is to evaluate whether surgical drain securement with a novel sutureless device (K-LOCKTM) will improve patient quality of life and reduce postoperative drain-related compl...
Detailed Description
Patients will be identified as potential subjects where the study team will speak with them, determine eligibility, and obtain consent prior to surgery. On the day of surgery, patients will be randomi...
Eligibility Criteria
Inclusion
- Age 18 years or older
- Patient of the Department of Plastic and Reconstructive Surgery
- Able to sign English language Consent form
- Undergoing a surgical procedure where placement of one or more surgical drains is anticipated
Exclusion
- Unable to sign English language consent form
- Incompatible drain size placed
- Allergy or sensitivity to skin adhesives
Key Trial Info
Start Date :
May 5 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
May 30 2027
Estimated Enrollment :
140 Patients enrolled
Trial Details
Trial ID
NCT06916286
Start Date
May 5 2025
End Date
May 30 2027
Last Update
May 29 2025
Active Locations (1)
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1
Wake Forest University Health Sciences
Winston-Salem, North Carolina, United States, 27157