DEBAKEY-CMR: DeBakey Cardiovascular Magnetic Resonance Study

Sponsor
Dipan Shah (Other)
Overall Status
Recruiting
CT.gov ID
NCT04281823
Collaborator
(none)
100,000
1
600
166.7

Study Details

Study Description

Brief Summary

While advancements in cardiac magnetic resonance (CMR) have improved image quality, it is unclear how these improvements are connected to the clinical evaluation of individuals with cardiovascular disease. The aim of this large prospective registry revolves around 4 key principles: 1) utilize CMR to gain additional pathophysiologic insights into cardiovascular disease, 2) understand how CMR compares to alternative cardiovascular diagnostic modalities, 3) determine how CMR affects clinical management decisions, and 4) establish a link between CMR findings and long term prognosis in patients with known or suspected cardiovascular disease. The ultimate aim is to utilize CMR to improve patient outcomes.

CMR techniques to be studies include function, fibrosis, and flow. Focus areas include valvular heart disease, ischemic heart disease, cardiomyopathies, and vascular disease.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Cardiovascular Magnetic Resonance

Detailed Description

Patient Population, Recruitment, and Consent:

Patients presenting to the Houston Methodist DeBakey CMR Laboratory will be enrolled from April 2008 to April 2038. It is expected that up to 100,000 patients may be enrolled during this period.

Subjects will be identified based on their referral to the Houston Methodist DeBakey CMR Laboratory for MRI studies during the proposed study period.

After enrollment, a registered nurse or physician will perform a thorough structured patient interview and/or review of electronic health records to document baseline medical history including cardiac risk factors, symptoms, medication usage, and prior procedure history. A small blood sample will be drawn and stored for future biomarker and/or genetic testing analysis. Annual follow up for clinical status will be performed via review of electronic health records; structured telephone interviews with the patients, relatives, and/or their health care providers; and/or the social security death index database.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
100000 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Houston Methodist DeBakey Cardiovascular Magnetic Resonance Study
Actual Study Start Date :
Apr 1, 2008
Anticipated Primary Completion Date :
Apr 1, 2058
Anticipated Study Completion Date :
Apr 1, 2058

Arms and Interventions

Arm Intervention/Treatment
Cardiovascular Magnetic Resonance

All patients who present to the Houston Methodist CMR Laboratory

Diagnostic Test: Cardiovascular Magnetic Resonance
Patients will undergo various CMR techniques designed to assess cardiovascular structure and function, tissue characteristics, and flow.

Outcome Measures

Primary Outcome Measures

  1. Mortality [Through study completion, an average of once a year, up to 20 years]

    All-cause mortality, Cardiovascular mortality (acute Myocardial Infarction, sudden death, heart failure, cerebrovascular, procedural), and Non-cardiovascular mortality

  2. Heart Failure [Through study completion, an average of once a year, up to 20 years]

    Congestive heart failure

  3. Heart and/or Lung Transplantation [Through study completion, an average of once a year, up to 20 years]

  4. Left Ventricular and/or Right Ventricular Assist Device Implantation [Through study completion, an average of once a year, up to 20 years]

Secondary Outcome Measures

  1. Cardiac Interventions [Through study completion, an average of once a year, up to 20 years]

    Implantable cardioverter-defibrillator (ICD), pacemakers, cardiac resynchronization therapy, coronary revascularization, valvular intervention, shunt closure

  2. Arrhythmic [Through study completion, an average of once a year]

    Sustained ventricular tachycardia, ventricular fibrillation, nonfatal cardiac arrest, appropriate ICD therapy

  3. Acute myocardial infarction [Through study completion, an average of once a year, up to 20 years]

  4. Acute Cerebrovascular Accident [Through study completion, an average of once a year, up to 20 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • All patients presenting to the Houston Methodist CMR Laboratory with known or suspected cardiovascular disease.
Exclusion Criteria:
  • Unable to provide informed consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 Houston Methodist Hospital Houston Texas United States 77030

Sponsors and Collaborators

  • Dipan Shah

Investigators

  • Principal Investigator: Dipan Shah, MD, The Methodist Hospital Research Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dipan Shah, Director of Cardiovascular Imaging, The Methodist Hospital Research Institute
ClinicalTrials.gov Identifier:
NCT04281823
Other Study ID Numbers:
  • Pro00008766
First Posted:
Feb 24, 2020
Last Update Posted:
Feb 24, 2020
Last Verified:
Feb 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dipan Shah, Director of Cardiovascular Imaging, The Methodist Hospital Research Institute
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 24, 2020