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NCT05903547 · ClinicalTrials.gov registry record · NA
A Skin Glue Versus Subcuticular Suture for Cesarean Closure Study
A NA study, sponsored by Columbia University.
- Completed
- Registry status
- NA
- Development phase
- 151
- Enrollment target
NCT05903547: Completed NA study, sponsored by Columbia University.
NCT05903547 is a NA study that has completed, run by Columbia University. The registered enrollment target is 151 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05903547, a NA study, has completed, sponsored by Columbia University.
- COMPLETED
- Registry status
- NA
- Development phase
- 151 participants
- Enrollment target
Study Summary
The aim of this study is to compare cesarean incision outcomes between patients with incision closed with the Dermabond Prineo system compared to standard subcuticular suture.
Primary Outcome
The patient's satisfaction with their cesarean incision will be assessed using the validated Patient Scar Assessment Scale (PSAS) questionnaire. The PSAS is a 6-item questionnaire that is scored on a 1 (no complaints/as normal skin) to 10 (worst imaginable/very different from normal skin) scale. Total scores range from 6-60, with a lower score indicating a greater level of patient satisfaction.
Interventions
- OTHER Suture
- DEVICE Dermabond Prineo
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 151 participants |
| Start Date | 2023-08-23 |
| Est. Completion | 2025-02-05 |
| Phase | NA |
What the finished NCT05903547 record still lists
NCT05903547 is an interventional study that assigns participants to a tested intervention. The registered 151 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (89% lower).
The record links to 0 conditions, and to 2 interventions - of which Suture is the first listed.
NCT05903547 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05903547 about?
NCT05903547 is a clinical study titled "A Skin Glue Versus Subcuticular Suture for Cesarean Closure Study". The aim of this study is to compare cesarean incision outcomes between patients with incision closed with the Dermabond Prineo system compared to standard subcuticular suture.
What is the current status of trial NCT05903547?
This trial is currently completed. It is a NA study. The enrollment target is 151 participants. The study started on 2023-08-23. Estimated completion is 2025-02-05.
What interventions are being tested in trial NCT05903547?
The interventions under investigation include: Suture (OTHER), Dermabond Prineo (DEVICE).
Who is sponsoring clinical trial NCT05903547?
This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05903547's enrollment target sits among peer trials
151 661st of 2000 higher than 1,340 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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