CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 22 enrolled
Drug / intervention
K-Lockdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT05251753
NCT05251753N/ACompleted
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Evaluation of a Novel Sutureless Drain Securement Device (K-Lock Device) and Comparison to Standard Suture-based Drain Securement Techniques

Wake Forest University Health Sciences·interventional·Posted Feb 23, 2022·Updated May 20, 2025

In Brief

A clinical study evaluating K-Lock for Skin Injury. Completed, enrolled 22 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsSkin Injury
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2023202420252026
First PostedFeb 23, 2022
Enrollment StartMar 7, 2022
Primary CompletionMar 6, 2025
TodayJul 2, 2026
Enrollment to primary: 3.0 yearsPosted 4.4 years ago

Interventions

K-Lockdevice

Patients will be randomized to either A) left side K-Lock with right side suture-based technique or B) right side K-Lock with left side suture-based technique.