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RECRUITING
NCT06916286
NA

Evaluating the Effect of Surgical Drain Securement on Patient Quality of Life and Postoperative Drain-related Complications

Sponsor: Wake Forest University Health Sciences

View on ClinicalTrials.gov

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 complications compared to drain securement with traditional suture-based methods. The K-LOCK™ Device is a novel sutureless drain securement device that may improve patient experiences with surgical drains.

Official title: A Prospective, Randomized, Multi-center Trial Evaluating the Effect of Surgical Drain Securement on Patient Quality of Life and Postoperative Drain-related Complications

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

140

Start Date

2025-05-05

Completion Date

2027-05-30

Last Updated

2026-02-25

Healthy Volunteers

No

Conditions

Interventions

DEVICE

K-Lock

Surgical drain securement with a novel sutureless K-LOCK device

OTHER

Suture

Surgical drain securement with traditional suture-based methods

Locations (1)

Wake Forest University Health Sciences

Winston-Salem, North Carolina, United States