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| 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 |
| 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 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 |
Patients suitable for Total Hip Resurfacing
Inclusion Criteria:
Exclusion criteria:
- less than 18 years of age
Contacts and Locations| United Kingdom | |
| Southmead Hospital | |
| Bristol, United Kingdom | |
| Robert Jones & Agnes Hunt Orthopaedic & District Hospital NHS Trust | |
| Oswestry, United Kingdom | |
| Principal Investigator: | Evert Smith, MD | North Bristol NHS Trust |
More Information
| 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: | May 4, 2012 |
| Health Authority: | United Kingdom: Medicines and Healthcare Products Regulatory Agency |
|
Arthritis Joint Diseases Musculoskeletal Diseases |