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ReCap Total Hip Resurfacing Prospective Data Collection

This study has been terminated.
Biomet U.K. Ltd.
Information provided by (Responsible Party):
Zimmer Biomet Identifier:
First received: September 23, 2008
Last updated: June 16, 2017
Last verified: June 2017
Prospective data collection on survivorship of ReCap Total Hip Resurfacing

Condition Intervention
Arthritis Device: ReCap Total Hip Resurfacing

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: ReCap Total Hip Resurfacing Prospective Data Collection

Further study details as provided by Zimmer Biomet:

Primary Outcome Measures:
  • survival rate [ Time Frame: 10 yr ]

Enrollment: 82
Study Start Date: March 2005
Study Completion Date: March 2010
Primary Completion Date: March 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Hip Resurfacing Device: ReCap Total Hip Resurfacing
ReCap Total Hip Resurfacing
Other Name: RECAP

Detailed Description:
Detailed protocol not available

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
Patients suitable for Total Hip Resurfacing

Inclusion Criteria:

  • Clinical diagnosis of hip joint arthritis

Exclusion criteria:

- less than 18 years of age

  Contacts and Locations
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Please refer to this study by its identifier: NCT00758472

United Kingdom
Southmead Hospital
Bristol, United Kingdom
Robert Jones & Agnes Hunt Orthopaedic & District Hospital NHS Trust
Oswestry, United Kingdom
Sponsors and Collaborators
Zimmer Biomet
Biomet U.K. Ltd.
Principal Investigator: Evert Smith, MD North Bristol NHS Trust
  More Information

Responsible Party: Zimmer Biomet Identifier: NCT00758472     History of Changes
Other Study ID Numbers: BMET UK 08
Study First Received: September 23, 2008
Last Updated: June 16, 2017 processed this record on September 21, 2017