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NCT02020018 · ClinicalTrials.gov registry record · NA
Negative Pressure Wound Therapy for Prevention of Poststernotomy Infection
A NA study, sponsored by Mayo Clinic.
- Completed
- Registry status
- NA
- Development phase
- 1,869
- Enrollment target
NCT02020018: Completed NA study, sponsored by Mayo Clinic.
NCT02020018 is a NA study that has completed, run by Mayo Clinic. The registered enrollment target is 1,869 participants. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02020018, a NA study, has completed, sponsored by Mayo Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 1,869 participants
- Enrollment target
Study Summary
This prospective study evaluates the role of negative pressure wound therapy or wound VAC as a dressing over the incision to prevent poststernotomy wound infection in high risk patients.
Interventions
- DEVICE Prevena Incision Management System
- OTHER Conventional sterile dry wound dressing
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,869 participants |
| Start Date | 2013-10 |
| Est. Completion | 2018-10 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02020018
The ClinicalTrials.gov registry entry for NCT02020018 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 1,869 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Mayo Clinic, which has 2,844 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Prevena Incision Management System is the first listed.
NCT02020018 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02020018 about?
NCT02020018 is a clinical study titled "Negative Pressure Wound Therapy for Prevention of Poststernotomy Infection". This prospective study evaluates the role of negative pressure wound therapy or wound VAC as a dressing over the incision to prevent poststernotomy wound infection in high risk patients.
What is the current status of trial NCT02020018?
This trial is currently completed. It is a NA study. The enrollment target is 1,869 participants. The study started on 2013-10. Estimated completion is 2018-10.
What interventions are being tested in trial NCT02020018?
The interventions under investigation include: Prevena Incision Management System (DEVICE), Conventional sterile dry wound dressing (OTHER).
Who is sponsoring clinical trial NCT02020018?
This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.
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