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This study has been withdrawn prior to enrollment.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.)
Information provided by (Responsible Party):
Biomet, Inc. Identifier:
First received: September 25, 2008
Last updated: December 2, 2011
Last verified: December 2011
Retrospective data collection of the CENOS implant comparing with and without BoneMaster HA coatings.


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

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Not applicable as study was withdrawn

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients Who Received CENOS prosthesis for Intended Uses
Patients Who Received CENOS prosthesis for Intended Uses
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

No Contacts or Locations Provided
  More Information

No publications provided

Responsible Party: Biomet, Inc. 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 processed this record on November 25, 2015