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The Impact of supplementation with L-carnitine in patients with heart disease undergoing cardiac surgery

The impact of supplementation with L-carnitine on left ventricular remodeling in patients with ischemic heart failure undergoing coronary artery bypass grafting - HF: Heart Failure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7376mq
Enrollment
Unknown
Registered
2014-08-19
Start date
2012-11-01
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Left ventricular dysfunction, heart failure, Myocardial Ischemia

Interventions

Patients with heart failure of ischemic etiology will be divided into two groups: supplemented and placebo group. The Group supplemented receive aqueous oral L-carnitine, providing 50mg/kg daily for 6
Dietary supplement

Sponsors

Universidade Federal Fluminense
Lead Sponsor
Universidade Federal Fluminense
Collaborator

Eligibility

Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Adults; lucid, oriented, both genders; greater than or equal to 18 years, less than or equal to 80 years, diagnosed with heart failure of ischemic etiology, NYHA functional class II and III; require coronary artery bypass grafting.

Exclusion criteria

Exclusion criteria: Renal dysfunction, hepatic dysfunction; disabsortive Syndromes; tumors, use of intra-aortic balloon; stroke, dysphagia, dialysis, sepsis, hemodynamic shock.

Design outcomes

Primary

MeasureTime frame
Increasing the ejection fraction of the left ventricle determined by echocardiography at the end of the study compared to the beginning.

Secondary

MeasureTime frame
Supplementation with L-carnitine in patients who present Ejection Fraction Left Ventricular lower than 50%, established by echocardiography.

Countries

Brazil

Contacts

Public ContactSheila Guimarães

Universidade Federal Fluminense

sheilamguimaraes@yahoo.com+55 (21) 988561844

Outcome results

None listed

Source: REBEC (via WHO ICTRP)