NCT07087210Active, not recruiting
In Vivo Quantitative Mapping of Mitochondrial Cardiac Membrane Potential in Heart Failure
Source: ClinicalTrials.gov · Last updated 25 Jul 2025
Brief summary (registry, in English)
This research aims to develop a new method to measure how well mitochondria are working using a special imaging technique called PET (positron emission tomography) with a tracer called 18F-TPP+. This tracer helps us visualize and measure mitochondrial function in a non-invasive way.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 30 (estimated)
- First submitted
- 28 Mar 2025
- Start date
- 25 Nov 2024
- Primary completion date
- Sept 2028
- Lead sponsor
- Matthieu Pelletier-Galarneau, MD MSc
- Diseases
- Heart failure
- NCT number
- NCT07087210
What you commit to
- Study type: Observational
- Planned participants: 30
- From 25 Nov 2024 to the primary completion date, Sept 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Lab values
- for all participants :
- Infiltrative CMP (e.g., cardiac amyloidosis)
- Hypertrophic CMP
- Dilated CMP
- Ischemic CMP with myocardial infarction
- Other chronic diseases or medications that may interfere with mitochondrial function
- Primary severe valvular disease
- Pericardial disease
- Pacemaker
- Defibrillator
- Congenital heart disease
- History of cardiac transplant
- BMI \>45 kg/m2
- High resting blood pressure ≥150/90 mmHg
- Estimated glomerular filtration rate (eGFR) \<50 mL/min/1.73m2
- Iodinated contrast allergy
- Women of child bearing potential
- Pregnancy
- Breastfeeding
- Inability to undergo the imaging logistics
- Any condition that, in the opinion of the investigator, could compromise the participation in the study
Who the study is looking for
- Active participants:
- ≥40 years old
- LVEF ≥50%
- Body Mass Index \<35kg/m2
- NYHA fuctional class I
- Engaged in aerobic exercise (running cycling or swimming) for ≥3 days per week or 5 hours per week without extensive layoff over the previous 6 months
- Non-smoker ≥1 year
- Fasting glycemia \<6.0 mmol/L
- HbA1c \<5.7%
- Sedentary participants:
- ≥40 years old
- LVEF ≥50%
- Body Mass Index \<35kg/m2
- NYHA fuctional class
- ≤1 structured physical activity per week
- Non-smoker ≥1 year
- Fasting glycemia \<6.0 mmol/L
- HbA1c \<5.7%
- HFpEF participants:
- Chronic symptomatic HF and LVEF \>40% within 12 months before the screening visit (regardless of the imaging modality)
- One of the following abnormalities:
- HF requiring hospitallization and IV diuretics within 12 months of study entry
- NTproBNP \>150 pg/ml in sinus rhythm
- NTproBNP \>450 pg/ml in chronic atrial fibrillation
Age in the registry: 40 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Montreal Heart Institute Coordinator of this site? Confirm its status | Montreal | Canada | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.