SUPARTZ Versus Placebo in Osteoarthritis of the Shoulder

Status Completed

Clinical Trial Summary

This clinical trial is to determine the safety and effectiveness of three injections of SUPARTZ (sodium hyaluronate) compared with phosphate buffered saline (PBS) for the treatment of glenohumeral osteoarthritis of the shoulder. The trial contains two phases. Phase I is 26 weeks, double blinded, and subjects are randomized to either SUPARTZ or PBS treatment. Phase II is 26 weeks (total 52 weeks) and open-label so all subjects will receive SUPARTZ injections only.

Clinical Trial Description

Phase 3 Study: Multi-center, randomized, double blinded, two phase study to determine the safety and efficacy of 3 injections of SUPARTZ for Osteoarthritis of the Shoulder ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00479687
Study type	Interventional
Source	Bioventus LLC
Contact
Status	Completed
Phase	N/A
Start date	May 2007
Completion date	October 2009

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