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NCT01446627 · ClinicalTrials.gov registry record
Use of Insorb Absorbable Vicryl Staples in Skin Closure for Cesarean Section
A clinical trial, sponsored by The University of Texas Health Science Center, Houston.
- Completed
- Registry status
- 300
- Enrollment target
NCT01446627 is a clinical trial that has completed, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 300 participants.
The verdict
NCT01446627 has completed, sponsored by The University of Texas Health Science Center, Houston.
- COMPLETED
- Registry status
- 300 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the incidence of wound breakdown or wound infection following skin closure with Insorb subcuticular absorbable staples versus metal staples after cesarean section through a retrospective chart analysis.
Interventions
- OTHER There is no intervention for this study
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 300 participants |
| Start Date | 2010-01 |
| Est. Completion | 2012-12 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01446627
The ClinicalTrials.gov registry entry for NCT01446627 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which There is no intervention for this study is the first listed.
NCT01446627 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01446627 about?
NCT01446627 is a clinical study titled "Use of Insorb Absorbable Vicryl Staples in Skin Closure for Cesarean Section". The purpose of this study is to evaluate the incidence of wound breakdown or wound infection following skin closure with Insorb subcuticular absorbable staples versus metal staples after cesarean section through a retrospective chart analysis.
What is the current status of trial NCT01446627?
This trial is currently completed. The enrollment target is 300 participants. The study started on 2010-01. Estimated completion is 2012-12.
What interventions are being tested in trial NCT01446627?
The interventions under investigation include: There is no intervention for this study (OTHER).
Who is sponsoring clinical trial NCT01446627?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
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