iCORE: Collaborative Orthopedics Outcomes Registry

SCRI Development Innovations, LLC

Overview

The goal of this registry is to review the data collected and research ways to improve patient safety, quality of care, and medical decision-making, reduce medical spending, and help advance orthopedic science and bioengineering.

Study Type

OBSERVATIONAL

Conditions

Arthroplasty, Replacement, Hip Arthroplasty, Replacement, Knee

Interventions

Patient RegistryOTHER

Orthopedic Data Registry

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * 18 years or older * Patients requested to be seen by an orthopedic surgeon participating in the iCORE Registry. * Patient must have the ability to understand the nature of the registry and give written informed consent. Exclusion Criteria: * There are no exclusion criteria for this Outcomes Registry.

Locations (1)

SCRI

Nashville, Tennessee, United States

Outcomes

Primary Outcomes

Quality Improvement

Time frame: 10 years

Treatment Patterns

Time frame: 5 years

Healthcare Utilization

Time frame: 5 years

Secondary Outcomes

Humanistic Outcomes

Time frame: 10 years

Economic Outcomes

Time frame: 10 years

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.