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NCT06412978 · ClinicalTrials.gov registry record · NA
Post-Operative Cesarean Section Cosmesis
A NA study of Cesarean Delivery, sponsored by Wake Forest University Health Sciences.
- Recruiting
- Registry status
- NA
- Development phase
- 52
- Enrollment target
- 1
- Study location
NCT06412978 is a NA study of Cesarean Delivery that is actively recruiting participants, run by Wake Forest University Health Sciences. The registered enrollment target is 52 participants, below the 3,478-participant average among 10 other Cesarean Delivery trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06412978, a NA study of Cesarean Delivery, is actively recruiting participants, sponsored by Wake Forest University Health Sciences.
- RECRUITING
- Registry status
- NA
- Development phase
- 52 participants
- Enrollment target
- 1
- Study location
Study Summary
Given the high numbers of cesarean deliveries being performed today, there has been interest in optimizing surgical techniques. Several recent reviews have summarized the evidence for various steps of cesarean delivery, but surprisingly in many cases there is little scientific evidence on which to base the choice of surgical technique.
Conditions Studied
Interventions
- PROCEDURE absorbable subcuticular polyglycolic acid staples (INSORB)
- PROCEDURE subcuticular, polyglecaprone suture (Monocryl)
Study Locations (1)
North Carolina
- Wake Forest University Health Sciences - Winston-Salem
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 52 participants |
| Start Date | 2024-09-05 |
| Est. Completion | 2026-10 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06412978
The ClinicalTrials.gov registry entry for NCT06412978 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 52 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,478-participant average among 10 other Cesarean Delivery trials with a reported enrollment target (99% lower). 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 Cesarean Delivery appearing as the primary indexed condition, and to 2 interventions - of which absorbable subcuticular polyglycolic acid staples (INSORB) is the first listed.
NCT06412978 reports 1 study location spanning 1 distinct geographic area - top geographies include North Carolina.
Frequently Asked Questions
What is clinical trial NCT06412978 about?
NCT06412978 is a clinical study titled "Post-Operative Cesarean Section Cosmesis". Given the high numbers of cesarean deliveries being performed today, there has been interest in optimizing surgical techniques. Several recent reviews have summarized the evidence for various steps of cesarean delivery, but surprisingly in many cases there is little scientific evidence on which to b...
What is the current status of trial NCT06412978?
This trial is currently recruiting. It is a NA study. The enrollment target is 52 participants. The study started on 2024-09-05. Estimated completion is 2026-10.
What conditions does trial NCT06412978 study?
This clinical trial studies the following conditions: Cesarean Delivery.
What interventions are being tested in trial NCT06412978?
The interventions under investigation include: absorbable subcuticular polyglycolic acid staples (INSORB) (PROCEDURE), subcuticular, polyglecaprone suture (Monocryl) (PROCEDURE).
Who is sponsoring clinical trial NCT06412978?
This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06412978 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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Read our methodology - how this data is sourced, computed, and verified.
Related
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