Actively Recruiting

All Genders
Healthy Volunteers
ID01909375

American Joint Replacement Registry Data Collection and Quality Improvement for Total Hip and Knee Replacements

Led by American Joint Replacement Registry · Updated on 2025-10-03

500000

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The American Joint Replacement Registry (AJRR) is a not-for-profit organization focused on collecting data and improving quality for total hip and knee replacement surgeries across the United States. This observational study collects information to support quality improvement efforts involving hospitals, surgeons, insurers, and device manufacturers. The registry is supported by several professional societies including the American Academy of Orthopaedic Surgeons and the American Association of Hip and Knee Surgeons. Participants are individuals undergoing total joint arthroplasty. Data is collected observationally without specific treatment assignments or interventions. The registry gathers information from various sources to monitor outcomes and quality measures related to joint replacement surgeries. Participants' health-related quality of life will be assessed at 12 months, along with specific measures like the Hip disability and Osteoarthritis Outcome Score - Joint Replacement (HOOS, JR). The study collects ongoing data to support improvements in joint replacement care while allowing participants to continue with their usual medical care. Participation duration varies depending on individual surgery and follow-up schedules.

CONDITIONS

Brief Title

American Joint Replacement Registry

Who Can Participate

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Any individual in the US undergoing total joint arthroplasty
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 12 months

Participants who undergo routine care are observed to collect data on health related quality of life and joint function following total hip or knee replacement.

Data collected at baseline and at 12 months

Trial Site Locations

Total: 1 location

1

Nathan Glusenkamp

Rosemont, Illinois, United States, 60018

Actively Recruiting

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Research Team

N

Nathan Glusenkamp

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Frequently Asked Questions

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