RecruitingEarly Phase 1NCT07201714

Oral Carnitine in Heart Failure Patients

Oral L-Carnitine Supplementation in Cardiorenal Heart Failure Patients


Sponsor

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

Enrollment

20 participants

Start Date

Nov 12, 2025

Study Type

INTERVENTIONAL

Conditions

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

Min Age: 18 Years

Inclusion Criteria5

  • 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 Criteria6

  • 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

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Interventions

DRUGLevocarnitine

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


Locations(1)

London Health Sciences Centre

London, Ontario, Canada

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NCT07201714


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