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NCT03136159 · ClinicalTrials.gov registry record · NA
The Role of Antimicrobial Foam Dressing in Prevention of Cesarean Section Wound Complications
A NA study of Cesarean Section; Complications, Wound, Dehiscence, sponsored by Loyola University.
- Completed
- Registry status
- NA
- Development phase
- 380
- Enrollment target
- 1
- Study location
NCT03136159 is a NA study of Cesarean Section; Complications, Wound, Dehiscence that has completed, run by Loyola University. The registered enrollment target is 380 participants. The trial reports 1 study location across 1 state.
The verdict
NCT03136159, a NA study of Cesarean Section; Complications, Wound, Dehiscence, has completed, sponsored by Loyola University.
- COMPLETED
- Registry status
- NA
- Development phase
- 380 participants
- Enrollment target
- 1
- Study location
Study Summary
Post-cesarean section wound infections are responsible for longer hospital stays, readmissions, and ultimately, increased costs to the healthcare system. Silver-containing dressings may prevent wound infections. The purpose of the current study is to determine if the use of a silver-impregnated dressing decreases the occurence of wound infection following cesarean delivery.
Conditions Studied
Interventions
- DEVICE Silver-impregnated antimicrobial dressing
Study Locations (1)
Illinois
- Loyola University Medical Center - Maywood
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 380 participants |
| Start Date | 2017-07-24 |
| Est. Completion | 2019-06-30 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03136159
The ClinicalTrials.gov registry entry for NCT03136159 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 380 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Loyola University, which has 92 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Cesarean Section; Complications, Wound, Dehiscence appearing as the primary indexed condition, and to 1 intervention - of which Silver-impregnated antimicrobial dressing is the first listed.
NCT03136159 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.
Frequently Asked Questions
What is clinical trial NCT03136159 about?
NCT03136159 is a clinical study titled "The Role of Antimicrobial Foam Dressing in Prevention of Cesarean Section Wound Complications". Post-cesarean section wound infections are responsible for longer hospital stays, readmissions, and ultimately, increased costs to the healthcare system. Silver-containing dressings may prevent wound infections. The purpose of the current study is to determine if the use of a silver-impregnated dres...
What is the current status of trial NCT03136159?
This trial is currently completed. It is a NA study. The enrollment target is 380 participants. The study started on 2017-07-24. Estimated completion is 2019-06-30.
What conditions does trial NCT03136159 study?
This clinical trial studies the following conditions: Cesarean Section; Complications, Wound, Dehiscence.
What interventions are being tested in trial NCT03136159?
The interventions under investigation include: Silver-impregnated antimicrobial dressing (DEVICE).
Who is sponsoring clinical trial NCT03136159?
This trial is sponsored by Loyola University, which has 92 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03136159 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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