Database of Patients Undergoing Cardiac Computed Tomographic Angiography at William Beaumont Hospital (CT DATABASE) (CTDATABASE)

This study is currently recruiting participants. (see Contacts and Locations)
Verified December 2013 by William Beaumont Hospitals
Sponsor:
Information provided by (Responsible Party):
Kavitha Chinnaiyan, William Beaumont Hospitals
ClinicalTrials.gov Identifier:
NCT00922662
First received: June 15, 2009
Last updated: December 12, 2013
Last verified: December 2013
  Purpose

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.


Condition
Acute Coronary Syndrome
Chest Pain

Study Type: Observational
Study Design: Observational Model: Cohort
Official Title: Database of Patients Undergoing Cardiac Computed Tomographic Angiography (CCTA)at William Beaumont Hospital

Resource links provided by NLM:


Further study details as provided by William Beaumont Hospitals:

Primary Outcome Measures:
  • 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 ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 10000
Study Start Date: December 2008
Estimated Study Completion Date: June 2019
Estimated Primary Completion Date: July 2017 (Final data collection date for primary outcome measure)
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.

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
  • Both genders
  • Retrospective CCTA subjects who have undergone CCTA in the past 5 years at this institution
  • Prospective subjects who will have a CCTA at this institution (ongoing)
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.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00922662

Contacts
Contact: Korana Stakich-Alpirez, BS, MS 248.898.0315 Korana.Stakich-Alpirez@beaumont.edu
Contact: Diedre Brunk, RN, MS,MBA 248.898.5580 diedre.brunk@beaumonthospitals.com

Locations
United States, Michigan
Beaumont Health System - Royal Oak Recruiting
Royal Oak, Michigan, United States, 48073
Contact: Korana Stakich-Alpirez, BS, MS    248-898-0315    Korana.Stakich-Alpirez@beaumont.edu   
Contact: Diedre Brunk, RN, MS,MBA    248.898.5580    diedre.brunk@beaumonthospitals.com   
Principal Investigator: Kavitha Chinnaiyan, MD         
Sponsors and Collaborators
Kavitha Chinnaiyan
Investigators
Principal Investigator: Kavitha Chinnaiyan, MD William Beaumont Hospital-Royal Oak
  More Information

No publications provided

Responsible Party: Kavitha Chinnaiyan, Director of Cardiovascular Imaging Education, William Beaumont Hospitals
ClinicalTrials.gov Identifier: NCT00922662     History of Changes
Other Study ID Numbers: 2009-021
Study First Received: June 15, 2009
Last Updated: December 12, 2013
Health Authority: United States: Institutional Review Board

Keywords provided by William Beaumont Hospitals:
coronary artery disease
chest pain
CCTA

Additional relevant MeSH terms:
Acute Coronary Syndrome
Chest Pain
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Angina Pectoris
Vascular Diseases
Pain
Signs and Symptoms

ClinicalTrials.gov processed this record on September 18, 2014