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Recruiting Early Phase 1

Oral Carnitine in Heart Failure Patients

NCT07201714 · tracked via the Priya Life Science Canada tracker
Phase
Early Phase 1
Started
2025-11-12
Last updated
2026-04-20

Condition(s) studied

Heart FailureCarnitine Deficiency

Investigational drug(s) / intervention(s)

Levocarnitine →

Levocarnitine: Oral L-carnitine, 2970mg daily (950mg, to be taken 3 times a day) for 3 months.

Study summary

Heart failure is a condition in which the heart is unable to pump blood effectively, leading to symptoms like being more tired, shortness of breath, and swelling in the body. Carnitine is a naturally occurring substance in the body that plays a role in turning fat into energy. This study will determine whether oral L-Carnitine supplementation can improve symptoms, enhance heart function and possibly improve the quality of life in individuals with heart failure.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Clinical-pathological diagnosis of heart failure with some degree of cardiorenal syndrome * Stage 1, 2, 3a, 3b, or 4 chronic kidney disease * Age ≥ 18 years * Able to speak and read English * Willing and able to provide consent Exclusion Criteria: * Estimated GFR \<15 mL/min/1.73m2 or Stage 5 chronic kidney disease * Currently undergoing renal replacement therapy of any kind * Pregnant, breastfeeding or intending pregnancy * History of seizures of any type * Known allergy to levocarnitine, magnesium stearate, microcrystalline cellulose or povidone * Unable to provide consent

Primary outcome measure(s)

  • Recruitment Rate — From study start to end of study at 52 weeks
    % of eligible patients enrolled over the study period
  • Retention Rate — From enrollment to end of treatment at 6 months
    % of enrolled participants completing final follow up
  • Intervention adherence — From enrollment to end of study treatment at 6 months
    Medication compliance measured by the % of prescribed L-carnitine doses taken. Pill counts will be completed at the end of the medication intervention time period at Visit 2.
  • Safety and Tolerability (adverse events) — From enrollment to end of treatment at 6 months
    Participants will be monitored throughout the study for any adverse events.
  • Data Completeness — From start of study to end of study at 52 weeks
    % of participants with complete data for each outcome

Trial sites (1)

FacilityCityRegionStatus
London Health Sciences Centre London Ontario Recruiting

More London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's trials in Canada

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 NCT07201714 on ClinicalTrials.gov ↗ ← All trials in Canada