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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: Clinical Trial NA study, sponsored by KCI USA.
NCT02302222 is a NA study that was terminated before completion, run by KCI USA. The registered enrollment target is 71 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Surgical Site Complications: * Dehiscence * Surgical site infection (SSI)
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 |
Why NCT02302222 stopped before completion
NCT02302222 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 71 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).
The record links to 0 conditions, and to 2 interventions - of which Standard of Care Dressing is the first listed.
NCT02302222 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02302222's enrollment target sits among peer trials
71 1102nd of 2000 higher than 898 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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