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NCT01357187 · ClinicalTrials.gov registry record · NA
An Evaluation of the Effect of the AmnioFix Amniotic Membrane Allograft in Patients Undergoing Posterior Instrumentation Removal
A NA study, sponsored by MiMedx Group.
- Completed
- Registry status
- NA
- Development phase
- 5
- Enrollment target
NCT01357187: Completed NA study, sponsored by MiMedx Group.
NCT01357187 is a NA study that has completed, run by MiMedx Group. The registered enrollment target is 5 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01357187, a NA study, has completed, sponsored by MiMedx Group.
- COMPLETED
- Registry status
- NA
- Development phase
- 5 participants
- Enrollment target
Study Summary
The objective of this study is to evaluate the clinical effectiveness of AmnioFix™ in the reduction of the tenacity and frequency of soft tissue adhesions during the removal of segmental posterior lumbar instrumentation.
Interventions
- OTHER Scheduled removal of posterior instrumentation with AmnioFix
- OTHER Scheduled removal of posterior instrumentation without AmnioFix
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 5 participants |
| Start Date | 2011-09 |
| Est. Completion | 2014-05 |
| Phase | NA |
What the finished NCT01357187 record still lists
NCT01357187 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).
The record links to 0 conditions, and to 2 interventions - of which Scheduled removal of posterior instrumentation with AmnioFix is the first listed.
NCT01357187 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01357187 about?
NCT01357187 is a clinical study titled "An Evaluation of the Effect of the AmnioFix Amniotic Membrane Allograft in Patients Undergoing Posterior Instrumentation Removal". The objective of this study is to evaluate the clinical effectiveness of AmnioFix™ in the reduction of the tenacity and frequency of soft tissue adhesions during the removal of segmental posterior lumbar instrumentation.
What is the current status of trial NCT01357187?
This trial is currently completed. It is a NA study. The enrollment target is 5 participants. The study started on 2011-09. Estimated completion is 2014-05.
What interventions are being tested in trial NCT01357187?
The interventions under investigation include: Scheduled removal of posterior instrumentation with AmnioFix (OTHER), Scheduled removal of posterior instrumentation without AmnioFix (OTHER).
Who is sponsoring clinical trial NCT01357187?
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 NCT01357187's enrollment target sits among peer trials
5 1988th of 2000 higher than 5 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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