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NCT02589210 · ClinicalTrials.gov registry record · NA
dHACM Mesh In the Treatment of Diabetic Foot Ulcers
A NA study, sponsored by MiMedx Group.
- Completed
- Registry status
- NA
- Development phase
- 10
- Enrollment target
NCT02589210: Completed NA study, sponsored by MiMedx Group.
NCT02589210 is a NA study that has completed, run by MiMedx Group. The registered enrollment target is 10 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02589210, a NA study, has completed, sponsored by MiMedx Group.
- COMPLETED
- Registry status
- NA
- Development phase
- 10 participants
- Enrollment target
Study Summary
A single-centered, non-randomized study with approximately 20 subjects that will be seen for up to 12 weeks, each receiving the EpiFix mesh plus standard of care. Safety and effectiveness will be monitored throughout the study.
Primary Outcome
The percentage of subjects with complete closure of the study ulcer as assessed by photographic evaluation
Interventions
- OTHER EpiFix Mesh
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2015-05 |
| Est. Completion | 2016-03 |
| Phase | NA |
What the finished NCT02589210 record still lists
NCT02589210 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which EpiFix Mesh is the first listed.
NCT02589210 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02589210 about?
NCT02589210 is a clinical study titled "dHACM Mesh In the Treatment of Diabetic Foot Ulcers". A single-centered, non-randomized study with approximately 20 subjects that will be seen for up to 12 weeks, each receiving the EpiFix mesh plus standard of care. Safety and effectiveness will be monitored throughout the study.
What is the current status of trial NCT02589210?
This trial is currently completed. It is a NA study. The enrollment target is 10 participants. The study started on 2015-05. Estimated completion is 2016-03.
What interventions are being tested in trial NCT02589210?
The interventions under investigation include: EpiFix Mesh (OTHER).
Who is sponsoring clinical trial NCT02589210?
This trial is sponsored by MiMedx Group, which has 32 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02589210's enrollment target sits among peer trials
10 1927th of 2000 higher than 26 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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