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A Retrospective Study of the iTotal CR Knee Replacement System
NCT01564654 · View on ClinicalTrials.gov ↗
Study Summary
This study involves retrospective collection of data regarding the first approximately 100 iTotal Knee Replacement System surgeries and their short term outcomes at a small set of centers throughout the US.
Conditions Studied
Interventions
- DEVICE iTotal KRS
Study Locations (4)
California
- STAR Orthopedics — La Quinta
Florida
- Preferred Orthopedics of the Palm Beaches — Boynton Beach
Tennessee
- Tennessee Orthopaedic Alliance — Nashville
Utah
- Central Utah Clinic — Provo
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 89 participants |
| Start Date | 2012-01 |
| Est. Completion | 2013-01 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01564654
The ClinicalTrials.gov registry entry for NCT01564654 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 89 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Restor3D, which has 4 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Osteoarthritis appearing as the primary indexed condition, and to 1 intervention — of which iTotal KRS 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: NCT01564654 reports 4 study locations spanning 4 distinct geographic areas — top geographies include California, Florida, Tennessee. 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 NCT01564654 about?
NCT01564654 is a clinical study titled "A Retrospective Study of the iTotal CR Knee Replacement System". This study involves retrospective collection of data regarding the first approximately 100 iTotal Knee Replacement System surgeries and their short term outcomes at a small set of centers throughout the US.
What is the current status of trial NCT01564654?
This trial is currently completed. The enrollment target is 89 participants. The study started on 2012-01. Estimated completion is 2013-01.
What conditions does trial NCT01564654 study?
This clinical trial studies the following conditions: Osteoarthritis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01564654?
The interventions under investigation include: iTotal KRS (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01564654?
This trial is sponsored by Restor3D, which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01564654 being conducted?
This trial has 4 study locations across California, Florida, Tennessee, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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