RECRUITING

Technical Development of Cardiovascular Magnetic Resonance Imaging

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Background: In the U.S., over 6.5 million people have heart failure. Researchers want to develop new testing methods for cardiovascular problems using magnetic resonance imaging (MRI) to improve the clinical diagnosis and management of people with heart failure. Objective: To develop and test new methods for imaging the heart and blood vessels using MRI. Eligibility: People ages 18 years and older who are having an MRI of their heart or blood vessels. Healthy volunteers are also needed. Design: Participants will be screened with a medical history. Participants will have a physical exam and blood tests. They will have an electrocardiogram (ECG) to measure the heart s electrical activity. Then they will have their scheduled MRI scan. The MRI scanner is a large, hollow tube. Participants will lie on a table that moves in and out of the tube. During the MRI, they may have contrast dye injected through an intravenous line inserted into their arm or hand. ECG may be used to monitor their heartbeat or coordinate pictures with their heartbeat. A flexible belt may be used to monitor their breathing. A finger probe may be used to track their heart rate and/or oxygenation level. Their blood pressure may be measured. Pictures may be taken of their blood vessels, heart, and lungs before, during, and after they get medicine to increase blood flow. They may lie flat and pedal a stress bicycle to increase their heart rate. Participation will last for 5 years. During that time, participants may receive a yearly survey about their health. They may be contacted for an optional follow-up MRI within 2 years of their MRI.

Official Title

Technical Development of Cardiovascular MRI

Quick Facts

Study Start:2024-04-08
Study Completion:2031-12-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04927429

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 100 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Provision of signed and dated informed consent form by subject
  2. * Stated willingness to comply with all study procedures and availability for the duration of the study
  3. * Male or female, 18 years or older
  4. * Subjects undergoing a clinically indicated MRI examination. Examples of medical indications include known or suspected heart failure or cardiomyopathy, chest pain with known or suspected coronary artery disease, unexplained dyspnea, valve disease, known or suspected congenital heart disease, cardiac masses and known or suspected aortic disease, exposure to cardiotoxic drugs, and systemic illnesses with known associated cardiovascular involvement.
  5. * Provision of signed and dated informed consent form
  6. * Stated willingness to comply with all study procedures and availability for the duration of the study
  7. * Male or female, 18 years or older
  1. 1. An individual who meets any of the following criteria will be excluded from participation in this study:
  2. * Unable to undergo magnetic resonance imaging because of:
  3. * Central nervous system aneurysm clips
  4. * Implanted neural stimulator
  5. * Implanted cardiac pacemaker or defibrillator
  6. * Cochlear implant
  7. * Ocular foreign body (e.g. metal shavings)
  8. * Implanted Insulin pump
  9. * Metal shrapnel or bullet
  10. * 2.For examinations that include contrast injection of GBCA:
  11. * For subjects with a planned pharmacological stress test with adenosine or regadenoson the following contraindications will be considered as

Contacts and Locations

Study Contact

Stacian D Awojoodu, C.R.N.P.
CONTACT
(240) 408-0498
stacian.davis@nih.gov
Eric E Morgan, M.D.
CONTACT
(419) 410-7079
eric.morgan2@nih.gov

Principal Investigator

Eric E Morgan, M.D.
PRINCIPAL_INVESTIGATOR
National Heart, Lung, and Blood Institute (NHLBI)

Study Locations (Sites)

Medstar Washington Hospital Center
Washington, District of Columbia, 20010
United States
National Institutes of Health Clinical Center
Bethesda, Maryland, 20892
United States

Collaborators and Investigators

Sponsor: National Heart, Lung, and Blood Institute (NHLBI)

  • Eric E Morgan, M.D., PRINCIPAL_INVESTIGATOR, National Heart, Lung, and Blood Institute (NHLBI)

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-04-08
Study Completion Date2031-12-31

Study Record Updates

Study Start Date2024-04-08
Study Completion Date2031-12-31

Terms related to this study

Keywords Provided by Researchers

  • Cardiac
  • Blood Pressure
  • HEART RATE
  • Heart Disease
  • Heart Failure
  • Natural History

Additional Relevant MeSH Terms

  • Cardiovascular Disease