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WithdrawnNCT03340233Updated May 1, 2019

Understanding the Mechanisms of Diastolic Dysfunction

An interventional study of MRI (cardiac) off-label use gadolinium contrast (IND exempt) and MRI (cardiac) in Heart Failure With Preserved Ejection Fraction and Healthy, sponsored by University of California, Los Angeles. Withdrawn at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2019-05-01.

Sponsored by University of California, Los Angeles · Not applicable, Interventional, and Diagnostic

Why this study was withdrawn
The PI left the institution and closed the study prior to enrolling any participants
Phase
Not applicable
Study type
Interventional
Enrollment
0
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
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Study summary

Heart failure is a clinical syndrome marked by breathlessness, even at low levels of exertion, general fatigue, and fluid retention and is estimated to affect 5.1 million people in the United States. Heart failure with preserved ejection fraction (HFpEF) means that the heart pumps enough blood to the body, but patients still have terrible symptoms. It is estimated to account for about 50% of all heart failure cases. Experts agree that impaired filling of the heart, perhaps due to "stiffness" of the heart muscle itself, critically underlies HFpEF. There is currently no clinical technique for measuring heart muscle (myocardial) stiffness; the very definition of "myocardial stiffness" remains poorly established. Consequently, the ability to study the mechanisms that underlie HFpEF is virtually non-existent, and limited treatment options will persist without significant advances. The objective of this project is to use an Equilibrium-Material-Stability (EMS) framework that couples patient-specific clinical MRI and heart pressure data in a computational model of the heart to diagnose changes in myocardial stiffness. The central hypothesis is that the new EMS framework for understanding the mechanisms of diastolic dysfunction in HFpEF will be more sensitive and outperform currently available approaches.

Read the detailed description

The study has three aims. The first aim of the project is to refine MRI techniques using "free-breathing" versus "breath-holding" measurements. Twenty-five normal volunteers will undergo MRI to refine "free-breathing" cardiac imaging and enable construction of patient-specific computer models of the heart. The second aim of the project is to validate and test the myocardial stiffness evaluation framework derived through the first objective in human subjects. Twenty-five normal volunteers will undergo MRI and the data from these images will be compared to specially constructed 3D printed models of the heart, enabling refinement of the EMS framework to separate structural stiffness from material stiffness. The third aim of the project is to measure changes in myocardial stiffness in patients with HFpEF. Thirty-three subjects with current diagnostic criteria for HFpEF will be evaluated at baseline and at six months to evaluate myocardial stiffness and cardiac MRI biomarkers. Specifically, this aim will establish the diagnostic sensitivity of the EMS framework with comparison to cardiac MRI biomarkers of increased stiffness, thereby providing mechanistic insight to one critical underlying cause of HFpEF.

02

Conditions studied

  • Heart Failure With Preserved Ejection Fraction
  • Healthy

Keywords

  • diastolic dysfunction
  • mechanism
  • MRI magnetic resonance imaging
  • ejection fraction
03

In context

Lead sponsor

University of California, Los Angeles is the lead sponsor of 1,167 studies on the registry; 192 are open to participants now.

Of its 95 completed or terminated interventional studies of FDA-regulated products, 69 (73%) have results posted.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria:

Healthy volunteers

1. Healthy adults

Patients with Heart Failure with Preserved Ejection Fraction

  1. Patient scheduled for catheterization at UCLA Medical Center
  2. Ejection fraction >/= 50%
  3. Signs and symptoms of heart failure
  4. Excluded other potential non-cardiac etiologies of heart failure

Exclusion Criteria:

Healthy volunteers

  1. Known medical condition that impacts heart health
  2. Contraindications to MRI (e.g., pacemaker/ICD, or claustrophobia)

Patients with Heart Failure with Preserved Ejection Fraction

Exclusion Criteria:

  1. Contraindications to MRI (e.g., pacemaker/ICD, or claustrophobia)
  2. Prior MI or history of PCI/CABG
  3. Worse than mild valvular disease
  4. Any indication for ICD implantation
  5. Contraindication to MRI contrast agents or eGRF \<30 ml/min/1.73m2 or MRI exams (e.g., pacemaker/ICD or claustrophobia).
  6. Atrial fibrillation or unstable cardiac rhythm
05

Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Group 1

    Group 1 includes 25 healthy subjects recruited in Year 1 to undergo cardiac MRI without contrast.

    Diagnostic Test: MRI (cardiac)

  • Experimental
    Group 2

    Group 2 includes 25 healthy subjects recruited in Year 2 to undergo cardiac MRI without contrast.

    Diagnostic Test: MRI (cardiac)

  • Experimental
    Group 3

    Group 3 includes 33 patients with Heart Failure with Preserved Ejection Fraction (HFpEF) who will undergo cardiac MRI at baseline and at six months to assess diagnostic sensitivity of MRI measurement.

    Diagnostic Test: MRI (cardiac) off-label use gadolinium contrast (IND exempt)

Interventions

  • Diagnostic testMRI (cardiac) off-label use gadolinium contrast (IND exempt)

    Clinical MRI

  • Diagnostic testMRI (cardiac)

    MRI without contrast

06

What researchers measure

Primary outcomes

  1. The sensitivity of the EMS framework with comparison to cardiac MRI biomarkers of increased stiffness, thereby providing mechanistic insight to one critical underlying cause of HFpEF.

    Assess the diagnostic sensitivity of MRI method by analyzing baseline and six month longitudinal characteristics in myocardial stiffness measured in patients with HFpEF

    Time frame: Five years

07

Study locations

1 site
  • University of California Los Angeles
    Los Angeles, California 90024, United States
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Jun 2018; primary completion for Sep 2021, 39 months later.

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

Registered
Nov 8, 2017
First posted
Nov 13, 2017
StartEst.
Jun 1, 2018
Primary completionEst.
Sep 2021
CompletionEst.
Aug 2022
Last update
May 1, 2019
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.
No changes since tracking began. The registry record was last updated on May 1, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03340233
Responsible party
Daniel Ennis, PhD (Associate Professor, University of California, Los Angeles) — Principal investigator
First posted
Nov 13, 2017
Start date
Jun 1, 2018 (estimated)
Primary completion
Sep 2021 (estimated)
Completion
Aug 2022 (estimated)
Last update
May 1, 2019

Study contacts

Daniel J Ennis, PhD
principal investigator · University of California, Los Angeles

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Apr 2019. You cannot join it, but the record below documents what was studied.

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