Heart's energy use revealed by new MRI technique in early trial
NCT ID NCT02648009
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-phase study tests a new MRI method that uses a special injection called hyperpolarized pyruvate to see how the heart uses energy. Researchers will scan the hearts of up to 112 people with high blood pressure, heart thickening, or heart failure. The goal is to see if this technique can show metabolic activity, which might help doctors better understand and manage heart conditions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Hyperpolarized Pyruvate (13C) Injection
- What this could lead to
- If successful, this imaging technique could help doctors see how the heart uses energy, potentially leading to better diagnosis and treatment of heart failure.
- What could go wrong
- This is a very early Phase 1 study focused on imaging, not treatment. It may not lead to any direct patient benefit, and the new method might not work as hoped in larger groups.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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About 112 people
The number the study aims to enrol. It can still change while the study runs.
- Start date
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Apr 2016
- Expected to finish
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Apr 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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19 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria * Written consent * Age: 19 to 50 in Arm 1, 30 to 75 in Arm 2 * Group 2A and 2E participants have left-ventricular hypertrophy * Group 2B and 2F participants have diagnosed hypertrophic cardiomyopathy * Group 2C and 2G participants are stable outpatients with NYHA class 1-3 heart failure with evidence of elevated LV mass (LVH), irrespective of LVEF. * Group 2D and 2H participants are stable patients with type 2 DM who have a HcA1c between 6.5-9% on oral hypoglycemic agents Exclusion Criteria * Contraindications to MRI or MRI contrast agents * Hemoglobin ≤ 9.0 gm/dL (only Group 2 participants) * Glomerular filtration rate (based on MDRD Equation) \< 30 ml/min/1.73m2 (only Group 2 participants) * Any condition leading to a life expectancy \<1 year * Medically diagnosed claustrophobia * Have received, or are scheduled to receive, another investigational medicinal product from 1 month prior to 1 month after inclusion in this study * BMI of less than 18.5 or greater than 32 * Group 1: medically diagnosed heart disease
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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St. Michael's Hospital
NOT_YET_RECRUITINGToronto, Ontario, Canada
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Sunnybrook Health Sciences Centre
RECRUITINGToronto, Ontario, M4N 3M5, Canada
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