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Retrospective Study on Cenos Stem With BoneMaster HA
This study is enrolling participants by invitation only.
Sponsored by: Biomet, Inc.
Information provided by: Biomet, Inc.
ClinicalTrials.gov Identifier: NCT00761046
  Purpose

Retrospective data collection of the CENOS implant comparing with and without BoneMaster HA coatings.


Condition
Total Hip Arthroplasty

U.S. FDA Resources
Study Type: Observational
Study Design: Cohort, Retrospective
Official Title: Retrospective Study on Cenos Stem With BoneMaster HA

Further study details as provided by Biomet, Inc.:

Primary Outcome Measures:
  • Complication Rate [ Designated as safety issue: Yes ]

Biospecimen Retention:   None Retained

Biospecimen Description:

Estimated Enrollment: 300
Study Start Date: October 2008
  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients Who Received CENOS prosthesis for Intended Uses

Criteria

Patients Who Received CENOS prosthesis for Intended Uses

  Contacts and Locations
No Contacts or Locations Provided
  More Information

Responsible Party: Biomet Germany ( Alexander Reiprich )
Study ID Numbers: BMET DE 02
Study First Received: September 25, 2008
Last Updated: September 25, 2008
ClinicalTrials.gov Identifier: NCT00761046  
Health Authority: Germany: Federal Institute for Drugs and Medical Devices

ClinicalTrials.gov processed this record on January 14, 2009