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Clinical Trials in Singapore / NCT06645691
Recruiting Phase 2

Hyperpolarized MR Imaging with Carbon-13 Pyruvate in the Human Body

NCT06645691 · tracked via the Priya Life Science Singapore tracker
Phase
Phase 2
Started
2024-10-17
Last updated
2024-12-06

Condition(s) studied

Heart FailureCardiometabolic SyndromeCancer DiagnosisCardiovascular DiseasesHealthy Volunteers

Investigational drug(s) / intervention(s)

Hyperpolarized 13C-pyruvate →

Hyperpolarized 13C-pyruvate: Hyperpolarized 13C-pyruvate is injected intravenously at a dose of 0.43 mL/kg body weight, and at a rate of 5 mL/second followed by a 20 mL saline flush at 5 mL/second when the patient is already in the MRI scanner

Study summary

Positron emission tomography with 18F fluorodeoxyglucose (FDG) is the conventional imaging technique to provide information regarding tissue glucose uptake and has been highly clinically successful. However, it cannot assess downstream metabolism, which may be useful in the diagnosis and assessment of treatment response in a variety of diseases. Patients will also be exposed to ionizing radiation, the amount of exposure can vary depending on the dose of tracer administered, frequency of scans and duration of each scan. Carbon-13 (13C) magnetic resonance imaging (MRI) is particularly attractive for metabolic imaging because carbon serves as the backbone of nearly all organic molecules in the body. With this technique, the polarization increases to approximately 30%-40%, an increase of over 10,000 to 100,000-fold, thereby dramatically increasing the MRI signal . Whilst the role of 13C imaging has been demonstrated in many sites around the world, we aim to demonstrate the feasibility and application of 13C hyperpolarized imaging in healthy Singapore residents and patients with cardiovascular and/or cardiometabolic diseases.

Eligibility

Sex
ALL
Min age
21 Years
Max age
99 Years
Healthy volunteers
Accepted
Inclusion Criteria: Healthy Volunteers: 1. Age 21 years and above 2. No significant medical co-morbidities (such as chronic kidney disease, diabetes mellitus, heart failure, ischemic heart disease, previous strokes) 3. No history of cancer 4. Able and willing to comply with study procedures and provide signed informed consent Patients with cardiovascular/cardiometabolic diseases: 1. Age 21 years and above 2. Physician diagnosed cardiovascular conditions: ischemic heart disease, inherited cardiomyopathies (hypertrophic, dilated or infiltrative cardiomyopathies) and stable heart failure; and/or 3. Cardiometabolic conditions (such as diabetes on medications, hypertension, central obesity, fatty liver disease) 4. Able and willing to comply with study procedures and provide signed informed consent Exclusion Criteria: 1. Standard contraindications for magnetic resonance procedures (such as implantable medical devices, suspected presence of surgical apparatus or shrapnel, severe claustrophobia) 2. Unstable medical conditions (such as symptomatic heart failure, unstable hypertension/glucose levels as determined by investigators, symptomatic arrhythmias, angina) 3. Pregnant or nursing women 4. Known allergies to pyruvate or any of its components

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
National Heart Centre Singapore Singapore Singapore Recruiting

More National Heart Centre Singapore trials in Singapore

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06645691 on ClinicalTrials.gov ↗ ← All trials in Singapore