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NCT03330041 · ClinicalTrials.gov registry record · NA
Suturing Distance From the Wound Edge, 2 mm vs 5 mm
A NA study of Cutaneous Sutures and Scar Cosmesis, sponsored by University of California, Davis.
- Completed
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT03330041 is a NA study of Cutaneous Sutures and Scar Cosmesis that has completed, run by University of California, Davis. The registered enrollment target is 50 participants. The trial reports 1 study location across 1 state.
The verdict
NCT03330041, a NA study of Cutaneous Sutures and Scar Cosmesis, has completed, sponsored by University of California, Davis.
- COMPLETED
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
This study aims to investigate whether the spacing of the interrupted cutaneous sutures affects surgical wound cosmesis on the face and neck. In other words, the investigators would like to determine which of the following yields a more cosmetically appealing scar: many closely approximated sutures or fewer, more widely spaced sutures. The investigators wish to compare the effects of two versus five millimeter spacing between sutures.
Conditions Studied
Interventions
- DEVICE Fast absorbing gut suture
Study Locations (1)
California
- University of California, Davis, Department of Dermatology - Sacramento
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2017-10-03 |
| Est. Completion | 2018-08-09 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03330041
The ClinicalTrials.gov registry entry for NCT03330041 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, Davis, which has 657 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Cutaneous Sutures and Scar Cosmesis appearing as the primary indexed condition, and to 1 intervention - of which Fast absorbing gut suture is the first listed.
NCT03330041 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT03330041 about?
NCT03330041 is a clinical study titled "Suturing Distance From the Wound Edge, 2 mm vs 5 mm". This study aims to investigate whether the spacing of the interrupted cutaneous sutures affects surgical wound cosmesis on the face and neck. In other words, the investigators would like to determine which of the following yields a more cosmetically appealing scar: many closely approximated sutures ...
What is the current status of trial NCT03330041?
This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2017-10-03. Estimated completion is 2018-08-09.
What conditions does trial NCT03330041 study?
This clinical trial studies the following conditions: Cutaneous Sutures and Scar Cosmesis.
What interventions are being tested in trial NCT03330041?
The interventions under investigation include: Fast absorbing gut suture (DEVICE).
Who is sponsoring clinical trial NCT03330041?
This trial is sponsored by University of California, Davis, which has 657 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03330041 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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