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ENROLLING BY INVITATION
NCT03404778

Comprehensive Reverse Shoulder Data Collection

Sponsor: Zimmer Biomet

View on ClinicalTrials.gov

Summary

This study is a multicenter, prospective, non-randomized, non-controlled clinical outcome study. The primary objective of this study is to evaluate improvement of pain score at one year for the Biomet Comprehensive Reverse Shoulder. The secondary objective is collection of long term clinical outcomes.

Official title: Comprehensive Reverse Shoulder Clinical Outcomes Study

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

175

Start Date

2010-03-07

Completion Date

2036-12

Last Updated

2025-10-30

Healthy Volunteers

No

Interventions

DEVICE

Biomet Comprehensive Reverse Shoulder

Designed to eliminate the potential for scapular notching, this reverse shoulder system combines a a true locking mechanism that minimized wear and oxidative breakdown with a modular central screw for secure fixation.

Locations (4)

Acromion LLC

Towson, Maryland, United States

William Beaumont Hospital

Royal Oak, Michigan, United States

Allina Health System DBA Sports and Orthopaedic Specialists

Edina, Minnesota, United States

Joint Implant Surgeons

New Albany, Ohio, United States