Maveric Magnetic Resonance Imaging Used to Study Detailed Bone Apposition and Fixation of the Stryker Trident II Tritanium System
Not Applicable
Completed
- Conditions
- Chronic Hip Pain
- Interventions
- Diagnostic Test: MRI
- Registration Number
- NCT03469817
- Lead Sponsor
- Hospital for Special Surgery, New York
- Brief Summary
The study aims to describe bone apposition and fixation of the Trident and Trident II Tritatnium acetabular system in patients 1 year status post total hip replacement. We will be studying this by comparing magnetic resonance imaging (MRI)s taken 1 year s/p total hip replacement with a Trident II cup with MRI's taken of patients with the Trident Cup who had MRIs done at 1 year post-op.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
- Patients who had a primary total hip replacement with a Stryker Trident II acetabular cup that have one year or more follow up.
- Patients that are willing able able to have an MRI at their one year follow up visit.
- Patients entered into the CORRe database (our HSS institutional joint replacement registry).
Exclusion Criteria
- Patients who have not been consented as part of the CORRe database.
- Patients who are unable or refuse to have an MRI at their 1 year follow up.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Patients who have undergone THR with Trident II Cup MRI Patients who have had THR with Trident II Cups and will have an MRI taken at their one year post-operative visit.
- Primary Outcome Measures
Name Time Method Comparison of bone apposition and fixation in patients with the Trident II Tritanium hip system with bone apposition and fixation in patients with Trident cups. 1 year
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Hospital for Special Surgery
🇺🇸New York, New York, United States