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iCORE: Collaborative Orthopedics Outcomes Registry (iCORE)

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ClinicalTrials.gov Identifier: NCT02422667
Recruitment Status : Recruiting
First Posted : April 21, 2015
Last Update Posted : May 3, 2017
Sponsor:
Information provided by (Responsible Party):
SCRI Development Innovations, LLC

Brief 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.

Condition or disease Intervention/treatment
Arthroplasty, Replacement, Hip Arthroplasty, Replacement, Knee Other: Patient Registry

Study Type : Observational [Patient Registry]
Estimated Enrollment : 10000 participants
Observational Model: Cohort
Time Perspective: Other
Target Follow-Up Duration: 10 Years
Official Title: iCORE: Collaborative Orthopedics Outcomes Registry
Actual Study Start Date : April 2015
Estimated Primary Completion Date : April 2020
Estimated Study Completion Date : April 2025

Intervention Details:
  • Other: Patient Registry
    Orthopedic Data Registry


Primary Outcome Measures :
  1. Quality Improvement [ Time Frame: 10 years ]
  2. Treatment Patterns [ Time Frame: 5 years ]
  3. Healthcare Utilization [ Time Frame: 5 years ]

Secondary Outcome Measures :
  1. Humanistic Outcomes [ Time Frame: 10 years ]
  2. Economic Outcomes [ Time Frame: 10 years ]


Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients 18 years and older who undergo hip and/or knee arthroplasty. Patient must have the ability to understand the nature of the registry and give written informed consent.
Criteria

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.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02422667


Contacts
Contact: Catherine Howard catherine.howard@sarahcannon.com

Locations
United States, Tennessee
SCRI Recruiting
Nashville, Tennessee, United States, 37203
Contact: Catherine Howard       catherine.howard@sarahcannon.com   
Principal Investigator: David K. DeBoer, MD         
Sponsors and Collaborators
SCRI Development Innovations, LLC
Investigators
Principal Investigator: David K DeBoer, MD SJRI/SCRI

Responsible Party: SCRI Development Innovations, LLC
ClinicalTrials.gov Identifier: NCT02422667     History of Changes
Other Study ID Numbers: SCRI HEOR_03
First Posted: April 21, 2015    Key Record Dates
Last Update Posted: May 3, 2017
Last Verified: May 2017

Keywords provided by SCRI Development Innovations, LLC:
Orthopedics
Outcome Assessment