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NCT04968405 · ClinicalTrials.gov registry record · NA

Catalyst CSR Shoulder System for Semi or Total Shoulder Arthroplasty

A NA study of Osteoarthritis Shoulder and Avascular Necrosis of the Head of Humerus, sponsored by Catalyst OrthoScience.

Recruiting
Registry status
NA
Development phase
90
Enrollment target
3
Study locations

NCT04968405 is a NA study of Osteoarthritis Shoulder and Avascular Necrosis of the Head of Humerus that is actively recruiting participants, run by Catalyst OrthoScience. The registered enrollment target is 90 participants, below the 359-participant average among 8 other Osteoarthritis Shoulder trials with a reported enrollment target (75% lower). The trial reports 3 study locations across 3 states.

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The verdict

NCT04968405, a NA study of Osteoarthritis Shoulder and Avascular Necrosis of the Head of Humerus, is actively recruiting participants, sponsored by Catalyst OrthoScience.

RECRUITING
Registry status
NA
Development phase
90 participants
Enrollment target
3
Study locations

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

Osteoarthritis Shoulder Avascular Necrosis of the Head of Humerus Rheumatoid Arthritis Shoulder

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

FieldValue
Enrollment Target 90 participants
Start Date 2022-07-22
Est. Completion 2026-02-28
Phase NA

Sponsor

Catalyst OrthoScience

1 total trials

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What the Registry Record Tells You About NCT04968405

The ClinicalTrials.gov registry entry for NCT04968405 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 359-participant average among 8 other Osteoarthritis Shoulder trials with a reported enrollment target (75% lower). The listed sponsor is Catalyst OrthoScience, which has 1 total studies on file at ClinicalTrials.gov.

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.

NCT04968405 reports 3 study locations spanning 3 distinct geographic areas - top geographies include Michigan, Oregon, Rhode Island.

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.

What interventions are being tested in trial NCT04968405?

The interventions under investigation include: Catalyst CSR Total Shoulder System (DEVICE).

Who is sponsoring clinical trial NCT04968405?

This trial is sponsored by Catalyst OrthoScience, which has 1 total clinical trials registered on ClinicalTrials.gov.

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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Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.