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Catalyst CSR Shoulder System for Semi or Total Shoulder Arthroplasty
NCT04968405 · View on ClinicalTrials.gov ↗
Study Summary
Evaluation of the performance and safety of the Catalyst CSR Shoulder System with clinical and radiographic results at multiple time points through 24 months postoperatively This study will be a prospective multi-center study conducted in the United States.
Conditions Studied
Interventions
- DEVICE Catalyst CSR Total Shoulder System
Study Locations (3)
Michigan
- Beaumont Hospital Royal Oak — Royal Oak
Oregon
- Kaiser Permanente Northwest Center for Health Research — Portland
Rhode Island
- Lifespan/University Orthopedics — Providence
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2022-07-22 |
| Est. Completion | 2026-02-28 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04968405
The ClinicalTrials.gov registry entry for NCT04968405 describes a study currently listed as recruiting. It is categorized as NA, 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 90 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Catalyst OrthoScience, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Osteoarthritis Shoulder appearing as the primary indexed condition, and to 1 intervention — of which Catalyst CSR Total Shoulder 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: NCT04968405 reports 3 study locations spanning 3 distinct geographic areas — top geographies include Michigan, Oregon, Rhode Island. 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 NCT04968405 about?
NCT04968405 is a clinical study titled "Catalyst CSR Shoulder System for Semi or Total Shoulder Arthroplasty". Evaluation of the performance and safety of the Catalyst CSR Shoulder System with clinical and radiographic results at multiple time points through 24 months postoperatively This study will be a prospective multi-center study conducted in the United States.
What is the current status of trial NCT04968405?
This trial is currently recruiting. It is a NA study. The enrollment target is 90 participants. The study started on 2022-07-22. Estimated completion is 2026-02-28.
What conditions does trial NCT04968405 study?
This clinical trial studies the following conditions: Osteoarthritis Shoulder, Avascular Necrosis of the Head of Humerus, Rheumatoid Arthritis Shoulder. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04968405?
The interventions under investigation include: Catalyst CSR Total Shoulder System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04968405?
This trial is sponsored by Catalyst OrthoScience, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04968405 being conducted?
This trial has 3 study locations across Michigan, Oregon, Rhode Island. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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