Mako-MORE Registry
Starting soon
Conditions studied: Arthropathy of Knee, Arthropathy of Hip
In brief
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.
Key facts
- Study ID
- NCT07647354
- Run by
- Stryker Orthopaedics
- People needed
- 950
- Starts
- 2026-06-15
- Expected to finish
- 2037-03-15
- Last updated by the study team
- 2026-06-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- The subject is skeletally mature, and ≥ 18 years old.
- The Subject has signed and dated an IRB/EC approved, study specific Informed Patient Consent Form (ICF).
- The subject is scheduled to undergo manual arthroplasty or Mako Robotic-Arm Assisted Arthroplasty according to IFU.
- The subject is willing and able to comply with postoperative scheduled clinical evaluations.
You may not qualify if…
- The subject is not able to express his/her consent as deemed by the investigator.
- The subject is not able to fulfill a self-assessment questionnaire or follow-up visits as deemed by the investigator.
- The subject is a prisoner.
- Per surgeon discretion the subject is not a candidate for the study.
- The subject is pregnant or breastfeeding.
Where it is running
- 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
Full record on ClinicalTrials.gov
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