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Mako-MORE Registry
Sponsor: Stryker Orthopaedics
Summary
This is a prospective, post-market, multi-center, registry-based observational study designed to collect real-world clinical data on patients undergoing joint arthroplasty with Stryker implants, with or without the use of the Mako Robotic-Arm Assisted System. The registry will collect prospective data on patient characteristics, procedural details, patient-reported outcomes, radiographic assessments, and adverse events. Patients will be enrolled into procedure-specific cohorts and followed for up to five years postoperatively.
Official title: A Prospective, Multi-center, Post-market, Registry-based Evaluation of the Clinical Outcomes in Patients Receiving a Stryker Implant With Use of the Mako Robotic-Arm Assisted System (Mako-MORE)
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
950
Start Date
2026-06-15
Completion Date
2037-03-15
Last Updated
2026-06-15
Healthy Volunteers
No
Conditions
Interventions
Mako Robotic-Arm Assisted Arthroplasty
This observational registry does not assign or mandate any intervention. Participants included in this group undergo hip or knee arthroplasty using the FDA-cleared Mako Robotic-Arm Assisted System as part of routine clinical care. Surgical approach, implant selection, and perioperative management are determined by the treating surgeon according to standard practice. Outcomes are observed prospectively without alteration to clinical care.
Locations (5)
Mayo Clinic (Jacksonville)
Jacksonville, Florida, United States
UofL Health
Louisville, Kentucky, United States
NYU Langone Orthopedic Hospital
New York, New York, United States
Cleveland Clinic
Cleveland, Ohio, United States
Ortho Rhode Island
Wakefield, Rhode Island, United States