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NCT06916286 · ClinicalTrials.gov registry record · NA
Evaluating the Effect of Surgical Drain Securement on Patient Quality of Life and Postoperative Drain-related Complications
A NA study of Surgical Drain, sponsored by Wake Forest University Health Sciences.
- Recruiting
- Registry status
- NA
- Development phase
- 140
- Enrollment target
- 1
- Study location
NCT06916286 is a NA study of Surgical Drain that is actively recruiting participants, run by Wake Forest University Health Sciences. The registered enrollment target is 140 participants. The trial reports 1 study location across 1 state.
The verdict
NCT06916286, a NA study of Surgical Drain, is actively recruiting participants, sponsored by Wake Forest University Health Sciences.
- RECRUITING
- Registry status
- NA
- Development phase
- 140 participants
- Enrollment target
- 1
- Study location
Study 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.
Conditions Studied
Interventions
- OTHER Suture
- DEVICE K-Lock
Study Locations (1)
North Carolina
- Wake Forest University Health Sciences - Winston-Salem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 140 participants |
| Start Date | 2025-05-05 |
| Est. Completion | 2027-05-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06916286
The ClinicalTrials.gov registry entry for NCT06916286 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 140 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Surgical Drain appearing as the primary indexed condition, and to 2 interventions - of which Suture is the first listed.
NCT06916286 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.
Frequently Asked Questions
What is clinical trial NCT06916286 about?
NCT06916286 is a clinical study titled "Evaluating the Effect of Surgical Drain Securement on Patient Quality of Life and Postoperative Drain-related Complications". 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...
What is the current status of trial NCT06916286?
This trial is currently recruiting. It is a NA study. The enrollment target is 140 participants. The study started on 2025-05-05. Estimated completion is 2027-05-30.
What conditions does trial NCT06916286 study?
This clinical trial studies the following conditions: Surgical Drain.
What interventions are being tested in trial NCT06916286?
The interventions under investigation include: Suture (OTHER), K-Lock (DEVICE).
Who is sponsoring clinical trial NCT06916286?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06916286 being conducted?
This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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