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COMPREHENSIVE® REVERSE SHOULDER Mini BasePlate

NCT02084693 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2019-07-05

No results posted yet for this study

Summary

Evaluate Survivorship for the Biomet® Comprehensive® Reverse Shoulder Mini Baseplate.

Conditions

  • Rotator Cuff Tear Arthropathy
  • Osteoporosis
  • Osteomalacia
  • Joint; Destruction, Sacroiliac

Interventions

DEVICE

COMPREHENSIVE

Comprehensive® Reverse Shoulder products are indicated for use in patients whose shoulder joint has a grossly deficient rotator cuff with severe arthropathy and/or previously failed shoulder joint replacement with a grossly deficient rotator cuff.

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Joo Han Oh, Ph.D. · Bundang Seoul Nat'l University Hospital

  • Sang Jin Shin, Ph.D. · Ewha Womans University Mokdong Hospital

  • Jae Chul Yoo, Ph. D. · Samsung Medical Center

  • Yong Girl Rhee, Ph.D. · Kyung Hee Univ. Hospital

  • Kyu Chul Noh, Ph.D. · Gangnam Sacred Heart Hospital

Eligibility

Min Age
60 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-12-31
Primary Completion
2019-04-30
Completion
2019-06-30

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02084693 on ClinicalTrials.gov