Last reviewed · How we verify

NCT06916286

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

Recruiting now NA Last updated 25 February 2026
What this trial tests

NA trial testing K-Lock in Surgical Drain in 140 participants. Currently enrolling.

Timeline
5 May 2025
Primary endpoint
30 May 2027
30 May 2027

Quick facts

Lead sponsorWake Forest University Health Sciences
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeother
Enrollment140
Start date5 May 2025
Primary completion30 May 2027
Estimated completion30 May 2027
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Wake Forest University Health Sciences

Who can join

18 and older, any sex, with Surgical Drain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

Verify or expand the search:

Other trials of K-Lock

Trials testing the same drug.

Other Wake Forest University Health Sciences trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06916286.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing