ClinicalTrials.gg
RecruitingNCT04927429Updated Oct 9, 2026

Technical Development of Cardiovascular Magnetic Resonance Imaging

An observational study in Cardiovascular Disease, sponsored by National Heart, Lung, and Blood Institute (NHLBI). Recruiting at 2 sites in United States. Open to participants aged 18 Years to 100 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-09.

Sponsored by National Heart, Lung, and Blood Institute (NHLBI) · Observational

From the registry’s dates

  • Started Apr 2024; still recruiting 2 years 7 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
3,400
Ages
18 Years to 100 Years
Sex
All
01

Study summary

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.

Read the detailed description

Study Desccription: This protocol allows testing of novel research pulse sequences in investigational cardiovascular magnetic resonance imaging (MRI) and allows application of custom pulse sequences that are not market-cleared in routine clinical MRI.

Objectives: To evaluate performance of novel pulse sequences for cardiovascular MRI in patients and healthy volunteers.

To provide a regulatory framework (abbreviated IDE) to implement and test custom pulse sequences (a non-significant risk medical device) in patients with cardiovascular disease.

Endpoints:

Primary Endpoint : Successful clinical performance of pulse sequences measured as the number of subjects with custom and novel pulse sequences that has provided diagnostic quality image.

Secondary Endpoint: Reference values in healthy volunteers for measurements of myocardial perfusion, T1, T2, and extracellular volume from custom pulse sequences.

Exploratory endpoints:

  • Differences in perfusion, function, infarction, extracellular volume, T1, T2 and T2*, flow with heart disease etiology, treatment and functional class of disease as well as age, sex, race and correlations between these parameters.
  • Relationship with clinical markers such as prognostic influence and change in patient management based on findings from MRI examination including the custom pulse sequences may be explored.
  • Comparisons to the results from novel and custom sequences to standard product sequences provided by the vendor may be performed.
  • To investigate the relationship between cardiac MRI biomarkers and blood biomarkers of heart disease in order to understand the disease process and enable a deep phenotyping of heart failure.
02

Conditions studied

  • Cardiovascular Disease

Keywords

  • Cardiac
  • Blood Pressure
  • HEART RATE
  • Heart Disease
  • Heart Failure
  • Natural History
03

In context

Cardiovascular Diseases

5,368 studies on the registry are indexed under Cardiovascular Diseases; 939 are open to participants now.

This study's planned enrollment of 3,400 is above the median of 506 across 1,572 observational studies indexed under Cardiovascular Diseases.

Browse Cardiovascular Diseases studies →

Lead sponsor

National Heart, Lung, and Blood Institute (NHLBI) is the lead sponsor of 1,143 studies on the registry; 71 are open to participants now.

Of its 58 completed or terminated interventional studies of FDA-regulated products, 51 (88%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 100 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Primary clinical

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

Group A: In order to be eligible to participate in this study, an individual must meet all of the following criteria:

  • Provision of signed and dated form by subject
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Male or female, 18 years or older
  • 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.

Group B, Healthy volunteers enrolled for developmental testing and establishing reference values for the custom pulse sequences. In order to be eligible to participate in this study, an individual must meet all of the following criteria:

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Male or female, 18 years or older

Exclusion criteria

EXCLUSION CRITERIA:

  1. An individual who meets any of the following criteria will be excluded from participation in this study:

    • Unable to undergo magnetic resonance imaging because of:

      • Central nervous system aneurysm clips
      • Implanted neural stimulator
      • Implanted cardiac pacemaker or defibrillator
      • Cochlear implant
      • Ocular foreign body (e.g. metal shavings)
      • Implanted Insulin pump
      • Metal shrapnel or bullet

    unless any of the above objects have been cleared as safe for MRI according to the assessment present as clinical routine at the site.

    • 2.For examinations that include contrast injection of GBCA:

      -- renal excretory dysfunction, estimated \<= 30 mL/min/1.73m(2) body surface area.(estimated glomerular filtration rate is only determined according to the institutional guidelines of patients at risk of renal dysfunction and may also depend upon the dose of GBCA administered).

      -- Known allergic reactions to GBCA

      -- Subjects may still be invited for non-contrast enhanced examinations or undergo MR examination with ferumoxytol as contrast agent.

      . For examinations that include contrast injection of ferumoxytol

      -- Known allergic reactions to ferumoxytol or to mannitol

    • For subjects with a planned pharmacological stress test with adenosine or regadenoson the following will be considered as exclusion criteria:

      --Bronchospastic lung disease with ongoing wheezing or history of significant reactive airway disease

      --Second- or third- degree atrioventricular blood, sinus node disease without a functioning MR conditional pacemaker

      --Systolic blood pressure \< 90 mmHg

      --Uncontrolled hypertension (systolic BP > 200 mmHg or diastolic BP > 110 mmHg)

      --Recent (\< 48hr) use of dipyridamole of dipyridamole- containing medications

      --Known to adenosine or regadenoson.

      • Unstable angina, acute coronary syndrome, or less than 2- 4 days after an acute myocardial infarction
      • For regadenoson only: seizure disorder as regadenoson may lower seizure threshold. Aminophylline should not be used in cases of seizures associated with Regadenoson.
    • Pregnant Women.
    • Lactating Women for administration of GBCA unless the subjects is willing to discard the milk for 24 hours after receiving gadolinium

    In addition, the following exclusion criteria pertains to Group B, healthy volunteers to be considered for reference values:

    • Known history of major illness, including, but not limited to having a hypertension diagnosis in need of anti-hypertensive medication, myocardial infarction, diabetes, familial hypercholesterolemia, cardiomyopathy, congenital heart disease, moderate or severe valvular disease, cerebrovascular insult or peripheral vascular disease, symptoms of angina or dyspnea, current smoker.
    • Decisionally impaired individuals
Terms in these criteria, in plain language(5)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

GFR and eGFR (kidney filtering)

GFR (glomerular filtration rate) is how much blood the kidneys filter each minute. It is usually estimated from a blood test — eGFR, by formulas such as CKD-EPI or MDRD — and some studies ask for it to be measured directly instead. Usually given in mL/min/1.73 m².

Check the method, the units and the minimum the study states. A value of 90 or above is in the normal-or-high range, but kidney damage can show in other tests too.

Excipients

The other ingredients in a medicine besides the active drug, such as fillers, colours or preservatives.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
3,400 participants (estimated)

Groups and cohorts

  • Affected participants

    Participants with a clinically indicated referral for cardiac MRI

  • Healthy participants

    Healthy individuals of various ethnicities to serve as reference ranges

06

What researchers measure

Primary outcomes

  1. To evaluate performance of novel pulse sequences for cardiovascular MRI in patients and healthy volunteers of both genders

    Clinical performance of pulse sequences measured as the number of subjects with custom and novel pulse sequences that has provided diagnostic quality image

    Time frame: 1 day

Secondary outcomes

  1. Establishing reference values for measurements from custom sequences.

    Reference values in healthy volunteers for measurements of heart filling and emptying measures, myocardial perfusion, T1, T2, T2\* and extracellular volume from custom pulse sequences.

    Time frame: 1 day

07

Study locations

2 of 2 sites recruiting
  • Medstar Washington Hospital Center
    Washington D.C., District of Columbia 20010, United States
    Recruiting
  • National Institutes of Health Clinical Center
    Bethesda, Maryland 20892, United States
    Recruiting
    • For more information at the NIH Clinical Center contact Office of Patient Recruitment (OPR) · Contactprpl@cc.nih.gov · 800-411-1222
08

References and documents

Individual participant data

Plan to share: Undecided

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Apr 2024 (actual). Primary completion is estimated for Aug 2027, 40 months after the start.

Of 580 non-industry observational studies under Cardiovascular Diseases, half reached primary completion within 70 months of starting (the median), counting those still running; a quarter within 28 and three quarters within 196. This study's planned 40 months is below that.

Counting every sponsor, half of 664 studies reached it within 61 months; a quarter within 24 and three quarters within 192.

Cardiovascular Diseases covers many different conditions, not one, so the studies compared here vary widely. Read these figures as a rough guide.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 15, 2021
First posted
Jun 16, 2021
StartActual
Apr 8, 2024
Primary completionEst.
Aug 31, 2027
CompletionEst.
Dec 31, 2031
Last update
Oct 9, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Minor edits
Nothing that changes what the study is or who can join. Edited: verification date
1 update, last Oct 9, 2026
Show all 1 update
  1. Oct 9, 2026
    Minor edits only
    + 1 other change: verification date

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT04927429
Responsible party
Sponsor
First posted
Jun 16, 2021
Start date
Apr 8, 2024
Primary completion
Aug 31, 2027 (estimated)
Completion
Dec 31, 2031 (estimated)
Last update
Oct 9, 2026

Study contacts

Stacian D Awojoodu, C.R.N.P.
Contact
stacian.davis@nih.gov
(240) 408-0498
Eric E Morgan, M.D.
Contact
eric.morgan2@nih.gov
(419) 410-7079
Eric E Morgan, M.D.
principal investigator · National Heart, Lung, and Blood Institute (NHLBI)

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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