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ReCap Total Hip Resurfacing Prospective Data Collection
This study is currently recruiting participants.
Verified September 2011 by Biomet, Inc.

First Received on September 23, 2008.   Last Updated on September 27, 2011   History of Changes
Sponsor: Biomet, Inc.
Collaborator: Biomet U.K. Ltd.
Information provided by (Responsible Party): Biomet, Inc.
ClinicalTrials.gov Identifier: NCT00758472
  Purpose

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 Biomet, Inc.:

Primary Outcome Measures:
  • survival rate [ Time Frame: 10 yr ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 500
Study Start Date: March 2005
Estimated Study Completion Date: March 2020
Estimated Primary Completion Date: March 2020 (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

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients suitable for Total Hip Resurfacing

Criteria

Inclusion Criteria:

  • Clinical diagnosis of hip joint arthritis

Exclusion criteria:

- less than 18 years of age

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

Locations
United Kingdom
Southmead Hospital Recruiting
Bristol, United Kingdom
Contact: E J Smith, FRCS     0117 950 5050        
Robert Jones & Agnes Hunt Orthopaedic & District Hospital NHS Trust Recruiting
Oswestry, United Kingdom
Contact: S Karlakki, FRCS     01691 404000        
Sponsors and Collaborators
Biomet, Inc.
Biomet U.K. Ltd.
Investigators
Principal Investigator: Evert Smith, MD North Bristol NHS Trust
  More Information

No publications provided

Responsible Party: Biomet, Inc.
ClinicalTrials.gov Identifier: NCT00758472     History of Changes
Other Study ID Numbers: BMET UK 08
Study First Received: September 23, 2008
Last Updated: September 27, 2011
Health Authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency

Additional relevant MeSH terms:
Arthritis
Joint Diseases
Musculoskeletal Diseases

ClinicalTrials.gov processed this record on February 09, 2012