iCORE: Collaborative Orthopedics Outcomes Registry

Arthroplasty, Replacement, Knee Clinical Trial

— iCORE  

Official title:

iCORE: Collaborative Orthopedics Outcomes Registry

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT02422667
• Other study ID #: SCRI HEOR_03
• Status: Withdrawn
• Start date: April 2015
• Est. completion date: April 2017

Study information

• Verified date: August 2020
• Source: SCRI Development Innovations, LLC
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: April 2017
• Est. primary completion date: April 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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.

Related Conditions & MeSH terms

• Arthroplasty, Replacement, Hip
• Arthroplasty, Replacement, Knee

Intervention

Other:
• Patient Registry
Orthopedic Data Registry

Locations

Country	Name	City	State
United States	SCRI	Nashville	Tennessee

Sponsors (1)

Lead Sponsor	Collaborator
SCRI Development Innovations, LLC

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Quality Improvement		10 years
Primary	Treatment Patterns		5 years
Primary	Healthcare Utilization		5 years
Secondary	Humanistic Outcomes		10 years
Secondary	Economic Outcomes		10 years