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NCT01528696 · ClinicalTrials.gov registry record · Phase 4
Silver Impregnated Dressings to Reduce Wound Complications in Obese Patients at Cesarean Section
A Phase 4 study, sponsored by University of Michigan.
- Terminated
- Registry status
- Phase 4
- Development phase
- 37
- Enrollment target
NCT01528696 is a Phase 4 study that was terminated before completion, run by University of Michigan. The registered enrollment target is 37 participants.
The verdict
NCT01528696, a Phase 4 study, was terminated before completion, sponsored by University of Michigan.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 37 participants
- Enrollment target
Study Summary
Obese patients undergoing cesarean section are at high risk for wound complications, which occur in approximately 20% of patients. This is a randomized controlled trial designed to determine whether the risk for wound-related complications can be reduced by covering the incision with a silver-impregnated dressing in the postoperative period.
Interventions
- DEVICE Silverlon
- DEVICE Standard Dressing
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 37 participants |
| Start Date | 2012-02 |
| Est. Completion | 2013-01 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01528696
The ClinicalTrials.gov registry entry for NCT01528696 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 37 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Michigan, which has 1,327 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Silverlon is the first listed.
NCT01528696 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01528696 about?
NCT01528696 is a clinical study titled "Silver Impregnated Dressings to Reduce Wound Complications in Obese Patients at Cesarean Section". Obese patients undergoing cesarean section are at high risk for wound complications, which occur in approximately 20% of patients. This is a randomized controlled trial designed to determine whether the risk for wound-related complications can be reduced by covering the incision with a silver-impreg...
What is the current status of trial NCT01528696?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 37 participants. The study started on 2012-02. Estimated completion is 2013-01.
What interventions are being tested in trial NCT01528696?
The interventions under investigation include: Silverlon (DEVICE), Standard Dressing (DEVICE).
Who is sponsoring clinical trial NCT01528696?
This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.
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