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NCT01552447 · ClinicalTrials.gov registry record · NA
Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers
A NA study of Venous Leg Ulcer, sponsored by MiMedx Group.
- Completed
- Registry status
- NA
- Development phase
- 98
- Enrollment target
- 5
- Study locations
NCT01552447 is a NA study of Venous Leg Ulcer that has completed, run by MiMedx Group. The registered enrollment target is 98 participants, below the 242-participant average among 35 other Venous Leg Ulcer trials with a reported enrollment target (60% lower). The trial reports 5 study locations across 4 states.
The verdict
NCT01552447, a NA study of Venous Leg Ulcer, has completed, sponsored by MiMedx Group.
- COMPLETED
- Registry status
- NA
- Development phase
- 98 participants
- Enrollment target
- 5
- Study locations
Study Summary
The purpose of this study is to determine whether the EpiFix human amniotic membrane is effective in the treatment of venous leg ulcers.
Conditions Studied
Interventions
- OTHER EpiFix
- OTHER Compression Therapy
Study Locations (5)
Pennsylvania
- St. Vincent's Health Center - Erie
- Armstrong County Memorial Hospital - Kittanning
Florida
- Eric J. Lullove DPM - Boca Raton
Massachusetts
- MetroWest Medical Center - Framingham
Oklahoma
- St. Johns Wound Center - Tulsa
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 98 participants |
| Start Date | 2012-03 |
| Est. Completion | 2014-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01552447
The ClinicalTrials.gov registry entry for NCT01552447 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 98 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 242-participant average among 35 other Venous Leg Ulcer trials with a reported enrollment target (60% lower). The listed sponsor is MiMedx Group, which has 32 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Venous Leg Ulcer appearing as the primary indexed condition, and to 2 interventions - of which EpiFix is the first listed.
NCT01552447 reports 5 study locations spanning 4 distinct geographic areas - top geographies include Pennsylvania, Florida, Massachusetts.
Frequently Asked Questions
What is clinical trial NCT01552447 about?
NCT01552447 is a clinical study titled "Human Amniotic Membrane Grafting and Standard of Care Versus Standard of Care Alone in the Treatment of Venous Leg Ulcers". The purpose of this study is to determine whether the EpiFix human amniotic membrane is effective in the treatment of venous leg ulcers.
What is the current status of trial NCT01552447?
This trial is currently completed. It is a NA study. The enrollment target is 98 participants. The study started on 2012-03. Estimated completion is 2014-05.
What conditions does trial NCT01552447 study?
This clinical trial studies the following conditions: Venous Leg Ulcer.
What interventions are being tested in trial NCT01552447?
The interventions under investigation include: EpiFix (OTHER), Compression Therapy (OTHER).
Who is sponsoring clinical trial NCT01552447?
This trial is sponsored by MiMedx Group, which has 32 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01552447 being conducted?
This trial has 5 study locations across Florida, Massachusetts, Oklahoma, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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