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NCT03533595 · ClinicalTrials.gov registry record · NA
Comparative Analysis of Sutures for Fascial Closure in Spinal Surgery
A NA study, sponsored by Thomas Jefferson University.
- Completed
- Registry status
- NA
- Development phase
- 20
- Enrollment target
NCT03533595 is a NA study that has completed, run by Thomas Jefferson University. The registered enrollment target is 20 participants.
The verdict
NCT03533595, a NA study, has completed, sponsored by Thomas Jefferson University.
- COMPLETED
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
Study Summary
STRATAFIX Symmetric PDS Plus sutures will reduce the time required for fascial closure following spinal surgery. A pilot study will aide in the design of a larger randomized controlled trial to compare suture closure time of the STRATAFIX Symmetric PDS Plus sutures versus traditional Vicryl sutures.
Interventions
- DEVICE Barbed
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2018-11-14 |
| Est. Completion | 2023-04-10 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03533595
The ClinicalTrials.gov registry entry for NCT03533595 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Thomas Jefferson University, which has 292 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Barbed is the first listed.
NCT03533595 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03533595 about?
NCT03533595 is a clinical study titled "Comparative Analysis of Sutures for Fascial Closure in Spinal Surgery". STRATAFIX Symmetric PDS Plus sutures will reduce the time required for fascial closure following spinal surgery. A pilot study will aide in the design of a larger randomized controlled trial to compare suture closure time of the STRATAFIX Symmetric PDS Plus sutures versus traditional Vicryl sutures.
What is the current status of trial NCT03533595?
This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2018-11-14. Estimated completion is 2023-04-10.
What interventions are being tested in trial NCT03533595?
The interventions under investigation include: Barbed (DEVICE).
Who is sponsoring clinical trial NCT03533595?
This trial is sponsored by Thomas Jefferson University, which has 292 total clinical trials registered on ClinicalTrials.gov.
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