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NCT01657474 · ClinicalTrials.gov registry record · NA
Comparative Study of Two Application Regimens of Amniotic Membrane Wound Graft In the Management of Diabetic Foot Ulcers
A NA study, sponsored by MiMedx Group.
- Completed
- Registry status
- NA
- Development phase
- 40
- Enrollment target
NCT01657474: Completed NA study, sponsored by MiMedx Group.
NCT01657474 is a NA study that has completed, run by MiMedx Group. The registered enrollment target is 40 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01657474, a NA study, has completed, sponsored by MiMedx Group.
- COMPLETED
- Registry status
- NA
- Development phase
- 40 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether a weekly application of EpiFix human amniotic membrane is more effective than a biweekly application (every two weeks) in the treatment of diabetic foot ulcers.
Interventions
- OTHER Weekly application of EpiFix plus standard of care
- OTHER Biweekly application of EpiFix plus standard of care
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2012-09 |
| Est. Completion | 2013-11 |
| Phase | NA |
What the finished NCT01657474 record still lists
NCT01657474 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 2 interventions - of which Weekly application of EpiFix plus standard of care is the first listed.
NCT01657474 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01657474 about?
NCT01657474 is a clinical study titled "Comparative Study of Two Application Regimens of Amniotic Membrane Wound Graft In the Management of Diabetic Foot Ulcers". The purpose of this study is to determine whether a weekly application of EpiFix human amniotic membrane is more effective than a biweekly application (every two weeks) in the treatment of diabetic foot ulcers.
What is the current status of trial NCT01657474?
This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2012-09. Estimated completion is 2013-11.
What interventions are being tested in trial NCT01657474?
The interventions under investigation include: Weekly application of EpiFix plus standard of care (OTHER), Biweekly application of EpiFix plus standard of care (OTHER).
Who is sponsoring clinical trial NCT01657474?
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 NCT01657474's enrollment target sits among peer trials
40 1447th of 2000 higher than 465 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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