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MIS MiLIF Versus Open
NCT00792129 · View on ClinicalTrials.gov ↗
Study Summary
This study is being undertaken to compare the clinical outcomes of patients that have unilateral posterolateral lumbar interbody fusion using a traditional open approach versus the MiLIF procedure based on the MiCOR Precision Bone Allograft, specialized Atavi instrumentation, and minimally invasive visualization capabilities.
Conditions Studied
Interventions
- DEVICE The Atavi System
Study Locations (9)
Florida
- Advanced Orthopedic Center — Port Charlotte
- Southeastern Spine Center — Sarasota
- Kennedy-White Orthopedic — Sarasota
California
- La Jolla Spine Institute — La Jolla
- Sharp Rees-Stealy Medical Group — San Diego
Oregon
- Oregon Brain & Spinal Institute — Portland
- Williamette Neurosurgery — Salem
Texas
- William Beaumont Army Medical Center — El Paso
Virginia
- Naval Medical Center — Portsmouth
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 113 participants |
| Start Date | 2004-04 |
| Est. Completion | 2009-06 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00792129
The ClinicalTrials.gov registry entry for NCT00792129 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 113 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Zimmer Biomet, which has 102 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Chronic Low Back Pain appearing as the primary indexed condition, and to 1 intervention — of which The Atavi System is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00792129 reports 9 study locations spanning 5 distinct geographic areas — top geographies include Florida, California, Oregon. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00792129 about?
NCT00792129 is a clinical study titled "MIS MiLIF Versus Open". This study is being undertaken to compare the clinical outcomes of patients that have unilateral posterolateral lumbar interbody fusion using a traditional open approach versus the MiLIF procedure based on the MiCOR Precision Bone Allograft, specialized Atavi instrumentation, and minimally invasive ...
What is the current status of trial NCT00792129?
This trial is currently completed. The enrollment target is 113 participants. The study started on 2004-04. Estimated completion is 2009-06.
What conditions does trial NCT00792129 study?
This clinical trial studies the following conditions: Chronic Low Back Pain, Leg Pain. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00792129?
The interventions under investigation include: The Atavi System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00792129?
This trial is sponsored by Zimmer Biomet, which has 102 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00792129 being conducted?
This trial has 9 study locations across California, Florida, Oregon, Texas, Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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