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Набира участници Ранна Фаза 1 NCT07201714

Oral Carnitine in Heart Failure Patients

Много ранно изпитване – основно за безопасност
Заболявания: Heart Failure Carnitine Deficiency

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

Налично на: БГ
Обобщение
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.
Описание
Heart failure (HF) is a multi-organ syndrome that is fundamentally driven by metabolic failure. Metabolic alterations include reduced fatty acid oxidation, which is the main fuel source for cardiac myocyctes in normal circumstances. Carnitine is a vitamin-like modified amino acid that is essential in the oxidation of fatty acids and has been found to be reduced in the heart failure population. Abnormalities in carnitine metabolism are thought to contribute to myocardial dysfunction, oxidative stress and inflammation. Carnitine supplementation may increase fatty acid oxidation, and therefore energy metabolism in heart failure patients, thus improving functional capacity, clinical measures and quality of life in this vulnerable patient population.
Кой може да участва
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
Интервенции
Levocarnitine
DRUG
Места на провеждане 1
Канада (1)
London Health Sciences Centre
London , Ontario
Технически детайли
Статус
Набира участници
Фаза
Ранна Фаза 1
Вид изследване
INTERVENTIONAL
Пол
Мъже и жени
Минимална възраст
18 Years
Здрави доброволци
Не
Начална дата
12.11.2025
Крайна дата
31.12.2026
Регистрационен номер
NCT07201714
Източник
clinicaltrials.gov
Запитване за медицински туризъм

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