CClinicalTrials.gg
Status unknownNCT01787812CJRRUpdated Jul 4, 2013

California Joint Replacement Registry

An observational study in Hip and Knee Replacement Surgeries, sponsored by California Joint Replacement Registry. Status unknown at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2013-07-04.

Sponsored by California Joint Replacement Registry · Observational

The sponsor has not verified this record recently (last verified Jul 2013), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
2,500
Ages
18 Years and older
Sex
All
01

Study summary

The California Joint Replacement Registry (CJRR) was created to meet the need for comprehensive, scientific assessment of devices, treatment protocols, surgical approaches, and patient factors influencing the results of hip and knee replacement surgeries. Importantly, it is a Level 3 registry, meaning it collects and incorporates clinical information and direct feedback from patients about the outcomes of hip and knee replacement surgeries. It is one of only a small number of registries in the United States to do so.

The CJRR's goals are to:

  • Collect and report scientifically valid data on the results of hip and knee replacements performed in California, including device safety and effectiveness, post-operative complication and revision rates, and patient-reported outcomes; and
  • Promote the use of performance information regarding hip and knee replacements to guide physician and patient decisions and to support programs for provider recognition and reward.

Specifically the CJRR is designed to:

  • Minimize burden on participants by using electronic data sources, rather than manual data entry or chart review.
  • Compile reports assessing the outcomes associated with different devices and surgical techniques.
  • Create benchmarking reports for physicians and hospitals that detail performance data and compare it to statewide averages.
  • Transmit safety alerts on devices with short-term results that provoke concern.
  • Shape a measurement and reporting system for total hip and total knee replacement surgeries.

The CJRR was developed by the California HealthCare Foundation (CHCF), the Pacific Business Group on Health (PBGH), and the California Orthopaedic Association (COA). PBGH manages the day-to-day operations of the CJRR.

CJRR's data elements are aligned with other major orthopedic registries. The CJRR is a member of the International Consortium of Orthopedic Registries (ICOR) and the International Society of Arthroscopic Registries (ISAR).

02

Conditions studied

  • Hip and Knee Replacement Surgeries
03

In context

Lead sponsor

This is the only study on the registry with California Joint Replacement Registry as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Californians, 18+ years of age, receiving hip or knee replacement surgery in California.

Inclusion criteria

  • Receiving hip or knee replacement surgery in California.

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
2,500 participants (estimated)
Target follow-up
5 Years
Patient registry
Yes
06

What researchers measure

Primary outcomes

  1. Number of Patients with Total Hip Replacement

    Time frame: 3 months, 6 months, every year up to 5 years

  2. Number of Patients with Partial Hip Replacement

    Time frame: 3 months, 6 months, every year up to 5 years

  3. Number of Patients with Hip Revision

    Time frame: 3 months, 6 months, every year up to 5 years

  4. Number of Patients with Total Knee Replacement

    Time frame: 3 months, 6 months, every year up to 5 years

  5. Number of Patients with Knee Revision

    Time frame: 3 months, 6 months, every year up to 5 years

Secondary outcomes

  1. Number and Type of Adverse Events as a Measure of Patient Safety

    Adverse Events: * Would infection * Fracture * Excessive bleeding * DVT proximal * DVT * PE * Congestive heart * Arrhythmia * Renal failure * Nerve injury * MI

    Time frame: 3 months

  2. Number and Type of Readmissions as a Measure of Surgical Quality

    Time frame: 3 months, 6 months, every year up to 5 years

  3. Number of Revisions as a Measure of Surgical Quality

    Time frame: 3 months, 6 months, every year up to 5 years

  4. Health-Related Quality of Life Score on the SF-12

    Time frame: 3 months, 6 months, every year up to 5 years

  5. Pain Score on the WOMAC

    Time frame: 3 months, 6 months, every year up to 5 years

  6. Stiffness Score on the WOMAC

    Time frame: 3 months, 6 months, every year up to 5 years

  7. Physical Function Score on the WOMAC

    Time frame: 3 months, 6 months, every year up to 5 years

  8. Activity Level Score on the UCLA Activity Index

    Time frame: 3 months, 6 months, every year up to 5 years

07

Study locations

1 of 1 sites recruiting
  • Hoag Orthopedic Institute
    Irvine, California 92618, United States
    • Kanoelani Allen, MSN-CNS, PHN, RN · Contact · kallen@hoag.org · 949.517.3138
    • James Caillouette, M.D. · Principal investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 4, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01787812
Lead sponsor
California Joint Replacement Registry
Responsible party
Sponsor
First posted
Feb 11, 2013
Start date
Jul 2011
Primary completion
Dec 2014 (estimated)
Last update
Jul 4, 2013

Study contacts

Rachel Brodie
Contact
rbrodie@pbgh.org
415.786.2204

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2013. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion