Retrospective Study on Cenos Stem With BoneMaster HA

This study has been withdrawn prior to enrollment.

(No data have been obtained at all in this time.)

Sponsor:

Information provided by (Responsible Party):

Biomet, Inc.

ClinicalTrials.gov Identifier:

NCT00761046

First received: September 25, 2008

Last updated: December 2, 2011

Last verified: December 2011

Purpose

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

Condition
Osteoarthritis

Study Type:	Observational
Study Design:	Observational Model: Cohort Time Perspective: Retrospective
Official Title:	Retrospective Study on Cenos Stem With BoneMaster HA

Resource links provided by NLM:

MedlinePlus related topics: Osteoarthritis

U.S. FDA Resources

Further study details as provided by Biomet, Inc.:

Primary Outcome Measures:

Complication Rate [ Time Frame: not available ] [ Designated as safety issue: Yes ]
not available

Enrollment:	0
Study Start Date:	October 2008

Detailed Description:

Not applicable as study was withdrawn

Eligibility

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

No publications provided

Responsible Party:	Biomet, Inc.
ClinicalTrials.gov Identifier:	NCT00761046 History of Changes
Other Study ID Numbers:	BMET DE 02
Study First Received:	September 25, 2008
Last Updated:	December 2, 2011
Health Authority:	Germany: Federal Institute for Drugs and Medical Devices

Additional relevant MeSH terms:

Osteoarthritis
Arthritis
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases

ClinicalTrials.gov processed this record on June 17, 2013