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Clinical Trials/NCT00922662
NCT00922662
Completed
Not Applicable

Database of Patients Undergoing Cardiac Computed Tomographic Angiography (CCTA)at William Beaumont Hospital

Kavitha Chinnaiyan1 site in 1 country10,000 target enrollmentDecember 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Acute Coronary Syndrome
Sponsor
Kavitha Chinnaiyan
Enrollment
10000
Locations
1
Primary Endpoint
To establish an overarching database of information containing historical, demographical, clinical, and intermediate and long-term outcome data from all WBH patients undergoing CCTA testing for clinical or scientific reasons.
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of the study is to establish an overarching database of information containing historical, demographical, clinical, and intermediate and long-term outcome data from all William Beaumont Hospital (WBH) patients undergoing Cardiac Computed Tomographic Angiography (CCTA) testing for clinical or scientific reasons.

Detailed Description

The principal goal of his project is to enable the study investigators to organize WBH research activity in the field of CCTA by concentrating data from all the patients who allow use of their data in one organized, audited and securely stored database. It will allow the ability to collect retrospective and prospective data from a number of different clinical systems and securely maintain patient medical record numbers for the reference on future projects as well as identification of patients with multiple studies and multiple follow-ups.

Registry
clinicaltrials.gov
Start Date
December 2008
End Date
September 2016
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Kavitha Chinnaiyan
Responsible Party
Sponsor Investigator
Principal Investigator

Kavitha Chinnaiyan

Director of Cardiovascular Imaging Education

William Beaumont Hospitals

Eligibility Criteria

Inclusion Criteria

  • all retrospective patients who under went a CTA and were granted a waiver of consent
  • all prospective patients CTA patients who gave informed consent.

Exclusion Criteria

  • Non CTA patients
  • Patients who refused participation.

Outcomes

Primary Outcomes

To establish an overarching database of information containing historical, demographical, clinical, and intermediate and long-term outcome data from all WBH patients undergoing CCTA testing for clinical or scientific reasons.

Time Frame: annually for 5 years

Study Sites (1)

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