- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01909375
American Joint Replacement Registry (AJRR)
September 30, 2025 updated by: Nathan Glusenkamp, American Joint Replacement Registry
The American Joint Replacement Registry is a not-for-profit 501(c)(3) organization for data collection and quality improvement initiatives for total hip and knee replacements.
The AJRR is a collaborative effort supported by the American Academy of Orthopaedic Surgeons (AAOS), the American Association of Hip and Knee Surgeons (AAHKS), The Hip Society, The Knee Society, hospitals, health insurers, medical device manufacturers, and contributions from individual orthopaedic surgeons.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
500000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Nathan Glusenkamp
- Phone Number: 8473844028
- Email: glusenkamp@aaos.org
Study Locations
-
-
Illinois
-
Rosemont, Illinois, United States, 60018
- Recruiting
- Nathan Glusenkamp
-
Contact:
- Nathan Glusenkamp
- Phone Number: 8473844028
- Email: glusenkamp@aaos.org
-
Contact:
- David G Lewallen, MD
- Email: lewallen.david@mayo.edu
-
Principal Investigator:
- Nathan Glusenkamp
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
We expect to receive data on up to 90% of all total joint arthroplasties conducted in the United States annually.
Description
Inclusion Criteria:
- Any individual in the US undergoing total joint arthroplasty
Exclusion Criteria:
- None
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Health Related Quality of Life
Time Frame: 12 months
|
Utilization of VR-12 and/or PROMIS-10
|
12 months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Hip disability and Osteoarthritis Outcome Score - Joint Replacement (HOOS, JR)
Time Frame: 12 months
|
12 months
|
Other Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Knee Injury and Osteoarthritis Outcome Score - Joint Replacement (KOOS, JR)
Time Frame: 12 months
|
12 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Nathan Glusenkamp, American Joint Replacement Registry
- Study Director: David G Lewallen, MD, American Joint Replacement Registry
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 1, 2011
Primary Completion (Estimated)
December 1, 2028
Study Completion (Estimated)
December 1, 2029
Study Registration Dates
First Submitted
July 24, 2013
First Submitted That Met QC Criteria
July 25, 2013
First Posted (Estimated)
July 26, 2013
Study Record Updates
Last Update Posted (Estimated)
October 3, 2025
Last Update Submitted That Met QC Criteria
September 30, 2025
Last Verified
September 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- 1120353
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
AJRR provides participating hospitals their data back in the form of dashboards and reports available on our registry platform.
AJRR also releases an Annual Report every November which includes aggregate, de-identified data.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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