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)
Facility
City
Region
Status
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
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.
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