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NCT02302222 · ClinicalTrials.gov registry record · NA
The Management of Closed Surgical Incisions Resulting From Incisional Hernia Repair and/or Functional Panniculectomy Using the Prevena™ Customizable™ Dressing
A NA study, sponsored by KCI USA.
- Terminated
- Registry status
- NA
- Development phase
- 71
- Enrollment target
NCT02302222 is a NA study that was terminated before completion, run by KCI USA. The registered enrollment target is 71 participants.
The verdict
NCT02302222, a NA study, was terminated before completion, sponsored by KCI USA.
- TERMINATED
- Registry status
- NA
- Development phase
- 71 participants
- Enrollment target
Study Summary
The goal of this study is to evaluate the impact of Customizable in the management of extensive closed surgical incisions for Subjects undergoing abdominal surgery for incisional hernia repair and/or functional panniculectomy as compared to SOC dressing, and to significantly reduce the SSC rate experienced by Subjects receiving Customizable vs. SOC surgical incision dressing.
Interventions
- DEVICE Standard of Care Dressing
- DEVICE Customizable Dressing with ActiV.A.C. Therapy Unit
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 71 participants |
| Start Date | 2015-05 |
| Est. Completion | 2017-07-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02302222
The ClinicalTrials.gov registry entry for NCT02302222 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 71 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is KCI USA, which has 11 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Standard of Care Dressing is the first listed.
NCT02302222 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02302222 about?
NCT02302222 is a clinical study titled "The Management of Closed Surgical Incisions Resulting From Incisional Hernia Repair and/or Functional Panniculectomy Using the Prevena™ Customizable™ Dressing". The goal of this study is to evaluate the impact of Customizable in the management of extensive closed surgical incisions for Subjects undergoing abdominal surgery for incisional hernia repair and/or functional panniculectomy as compared to SOC dressing, and to significantly reduce the SSC rate expe...
What is the current status of trial NCT02302222?
This trial is currently terminated. It is a NA study. The enrollment target is 71 participants. The study started on 2015-05. Estimated completion is 2017-07-31.
What interventions are being tested in trial NCT02302222?
The interventions under investigation include: Standard of Care Dressing (DEVICE), Customizable Dressing with ActiV.A.C. Therapy Unit (DEVICE).
Who is sponsoring clinical trial NCT02302222?
This trial is sponsored by KCI USA, which has 11 total clinical trials registered on ClinicalTrials.gov.
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