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NCT04339439 · ClinicalTrials.gov registry record · NA
Does Addition of a Vessel Loop in Wound Closure Improve Suture Removal?
A NA study, sponsored by Carilion Clinic.
- Terminated
- Registry status
- NA
- Development phase
- 47
- Enrollment target
NCT04339439: Clinical Trial NA study, sponsored by Carilion Clinic.
NCT04339439 is a NA study that was terminated before completion, run by Carilion Clinic. The registered enrollment target is 47 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04339439, a NA study, was terminated before completion, sponsored by Carilion Clinic.
- TERMINATED
- Registry status
- NA
- Development phase
- 47 participants
- Enrollment target
Study Summary
This study will investigate whether adding a vessel loop under sutures after elective carpal tunnel release increases patient satisfaction with suture removal.
Primary Outcome
This will be measured on a 100mm visual analog scale.
Interventions
- DEVICE Vessel loop (FDA product code FZZ)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 47 participants |
| Start Date | 2020-08-01 |
| Est. Completion | 2022-07-19 |
| Phase | NA |
Why NCT04339439 stopped before completion
NCT04339439 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 47 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 1 intervention - of which Vessel loop (FDA product code FZZ) is the first listed.
NCT04339439 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT04339439 about?
NCT04339439 is a clinical study titled "Does Addition of a Vessel Loop in Wound Closure Improve Suture Removal?". This study will investigate whether adding a vessel loop under sutures after elective carpal tunnel release increases patient satisfaction with suture removal.
What is the current status of trial NCT04339439?
This trial is currently terminated. It is a NA study. The enrollment target is 47 participants. The study started on 2020-08-01. Estimated completion is 2022-07-19.
What interventions are being tested in trial NCT04339439?
The interventions under investigation include: Vessel loop (FDA product code FZZ) (DEVICE).
Who is sponsoring clinical trial NCT04339439?
This trial is sponsored by Carilion Clinic, which has 45 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT04339439's enrollment target sits among peer trials
47 1400th of 2000 higher than 599 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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