Clinical Study Evaluating an Acetabular Cup System After Total Hip Replacement
Primary Purpose
Osteoarthritis, Rheumatoid Arthritis, Arthritis
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Acetabular cup
Sponsored by
About this trial
This is an interventional treatment trial for Osteoarthritis focused on measuring Total Hip Replacement, post-traumatic arthritis
Eligibility Criteria
Inclusion Criteria: Primary hip replacement Sufficient bone stock to support implant Signed Informed Patient Consent form Exclusion Criteria: Prior renal transplant History of active joint sepsis Recent high dose of corticosteroids Primary or secondary carcinoma in the last 5 years Neurological disease Psychosocial disease that would limit rehabilitation Use of structural bone graft Simultaneous participation in another hip study
Sites / Locations
- DePuy Orthopaedics
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
A
Arm Description
Acetabular cup replacement with total hip arthroplasty
Outcomes
Primary Outcome Measures
Survivorship
Secondary Outcome Measures
Harris Hip Score
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)
Short Form-36 (SF-36)
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00306930
Brief Title
Clinical Study Evaluating an Acetabular Cup System After Total Hip Replacement
Official Title
Multi-center, Prospective, Clinical Evaluation of Pinnacle Acetabular Implants in Total Hip Arthroplasty
Study Type
Interventional
2. Study Status
Record Verification Date
July 2014
Overall Recruitment Status
Completed
Study Start Date
July 2000 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
December 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
DePuy Orthopaedics
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study is a clinical evaluation of survivorship of an acetabular cup system after total hip replacement using patient examinations and questionnaires.
Detailed Description
The primary objective of this investigation is to evaluate survivorship at five years of the Pinnacle™ acetabular cup system in primary total hip arthroplasty.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Rheumatoid Arthritis, Arthritis, Avascular Necrosis, Acute Fracture
Keywords
Total Hip Replacement, post-traumatic arthritis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
1593 (Actual)
8. Arms, Groups, and Interventions
Arm Title
A
Arm Type
Other
Arm Description
Acetabular cup replacement with total hip arthroplasty
Intervention Type
Device
Intervention Name(s)
Acetabular cup
Other Intervention Name(s)
Pinnacle™ Cup
Intervention Description
Acetabular cup replacement
Primary Outcome Measure Information:
Title
Survivorship
Time Frame
5 years
Secondary Outcome Measure Information:
Title
Harris Hip Score
Time Frame
Pre-operative, 6 month and 1, 2, 3, 4, and 5 years.
Title
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)
Time Frame
Pre-operative, 6 month and 1, 2, 3, 4 and 5 years.
Title
Short Form-36 (SF-36)
Time Frame
Pre-operative, 6 month and 1, 2, 3, 4 and 5 years.
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Primary hip replacement
Sufficient bone stock to support implant
Signed Informed Patient Consent form
Exclusion Criteria:
Prior renal transplant
History of active joint sepsis
Recent high dose of corticosteroids
Primary or secondary carcinoma in the last 5 years
Neurological disease
Psychosocial disease that would limit rehabilitation
Use of structural bone graft
Simultaneous participation in another hip study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dave Whalen, BS, DC
Organizational Affiliation
DePuy Orthopaedics
Official's Role
Study Director
Facility Information:
Facility Name
DePuy Orthopaedics
City
Warsaw
State/Province
Indiana
ZIP/Postal Code
46581
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Clinical Study Evaluating an Acetabular Cup System After Total Hip Replacement
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