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NCT05251753 · ClinicalTrials.gov registry record · NA

Evaluation of a Novel Sutureless Drain Securement Device

A NA study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
NA
Development phase
22
Enrollment target

NCT05251753: Completed NA study, sponsored by Wake Forest University Health Sciences.

NCT05251753 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 22 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05251753, a NA study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
NA
Development phase
22 participants
Enrollment target

Study 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.

Primary Outcome

Time it takes to secure and dress each drain will be evaluated in totality by evaluation of video recordings to record timestamps and documented on "K-Lock Study Outcomes" tool. This will help determine the feasibility of using this device.

Interventions

  • DEVICE K-Lock

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2022-03-07
Est. Completion 2025-03-06
Phase NA
Wake Forest University Health Sciences

1,140 total trials

What the finished NCT05251753 record still lists

NCT05251753 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 1 intervention - of which K-Lock is the first listed.

NCT05251753 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05251753 about?

NCT05251753 is a clinical study titled "Evaluation of a Novel Sutureless Drain Securement Device". The purpose of this study is to evaluate an investigational sutureless drain securement device (K-Lock) and compare this device to standard drain securement.

What is the current status of trial NCT05251753?

This trial is currently completed. It is a NA study. The enrollment target is 22 participants. The study started on 2022-03-07. Estimated completion is 2025-03-06.

What interventions are being tested in trial NCT05251753?

The interventions under investigation include: K-Lock (DEVICE).

Who is sponsoring clinical trial NCT05251753?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05251753's enrollment target sits among peer trials

22 1756th of 2000 higher than 239 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05251753, the US trial registry maintained by the National Library of Medicine. NCT05251753 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.