iCORE: Collaborative Orthopedics Outcomes Registry

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2015-04-30

Study Completion Date

2017-04-30

Brief Summary

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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.

Detailed Description

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Conditions

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Arthroplasty, Replacement, Hip Arthroplasty, Replacement, Knee

Keywords

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Orthopedics Outcome Assessment

Study Design

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Observational Model Type

COHORT

Study Time Perspective

OTHER

Interventions

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Patient Registry

Orthopedic Data Registry

Intervention Type OTHER

Eligibility Criteria

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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.

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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David K DeBoer, MD

Role: PRINCIPAL_INVESTIGATOR

SJRI/SCRI

Locations

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SCRI

Nashville, Tennessee, United States

Site Status

Countries

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United States

Other Identifiers

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SCRI HEOR_03

Identifier Type: -

Identifier Source: org_study_id