NCT02422667

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.

Trial Health

30
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Timeline
Completed

Started Apr 2015

Geographic Reach
1 country

1 active site

Status
withdrawn

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 1, 2015

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

April 14, 2015

Completed
7 days until next milestone

First Posted

Study publicly available on registry

April 21, 2015

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2017

Completed
Last Updated

December 5, 2023

Status Verified

August 1, 2020

Enrollment Period

2 years

First QC Date

April 14, 2015

Last Update Submit

December 1, 2023

Conditions

Arthroplasty, Replacement, HipArthroplasty, Replacement, Knee

Keywords

OrthopedicsOutcome Assessment

Outcome Measures

Primary Outcomes (3)

  • Quality Improvement

    10 years

  • Treatment Patterns

    5 years

  • Healthcare Utilization

    5 years

Secondary Outcomes (2)

  • Humanistic Outcomes

    10 years

  • Economic Outcomes

    10 years

Interventions

Patient RegistryOTHER

Orthopedic Data Registry

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability 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.

You may qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

SCRI

Nashville, Tennessee, 37203, United States

Location

Study Officials

  • David K DeBoer, MD

    SJRI/SCRI

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Target Duration
10 Years
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 14, 2015

First Posted

April 21, 2015

Study Start

April 1, 2015

Primary Completion

April 1, 2017

Study Completion

April 1, 2017

Last Updated

December 5, 2023

Record last verified: 2020-08

Locations

US(1)