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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 is a NA study that has completed, run by MiMedx Group. The registered enrollment target is 5 participants.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01357187
The ClinicalTrials.gov registry entry for NCT01357187 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 5 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is MiMedx Group, which has 32 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Scheduled removal of posterior instrumentation with AmnioFix is the first listed.
NCT01357187 reports 0 study locations.
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.
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