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Effect of Carnitine on Uremic Cardiomyopathy

T

Toujinkai Hospital

Status

Completed

Conditions

Disorder of Fatty Acid Metabolism

Treatments

Drug: Intravenous administration of L-carnitine

Study type

Interventional

Funder types

Other

Identifiers

NCT02322697
Dialysis heart carnitine study

Details and patient eligibility

About

Patients on chronic hemodialysis without obstructive coronary artery disease identified by coronary angiography were randomly divided into the two groups: carnitine group and control group. SPECT using FFA analogue, BMIPP, was performed before and one year after intravenous administration of L-carnitine (1000 mg on every dialysis session). Control group received the examination of BMIPP SPECT at the same time of the carnitine group. The effects of chronic intravenous administration of L-carnitine on myocardial fatty acid metabolism were investigated among this population.

Full description

Patients on chronic hemodialysis in Toujinkai hospital who had no obstructive coronary artery disease identified by coronary angiography and left ventricular dysfunction were randomly divided into the two groups: carnitine group and control group. To evaluate the possible effect of carnitine administration on myocardial fatty acid metabolism, SPECT using FFA analogue, BMIPP, was performed before and one year after intravenous administration of L-carnitine (1000 mg on every dialysis session). Control group received the examination of BMIPP SPECT at the same time of the carnitine group. Circulating concentrations of total, free, and acyl L-carnitine were measured every three months in the carnitine group. Clinical data including blood chemistry, blood pressure, or cardiac functions by echocardiography were obtained every 6 months in both groups. The effects of chronic intravenous administration of L-carnitine on myocardial fatty acid metabolism and cardiac functions were investigated among this population.

Enrollment

60 patients

Sex

All

Ages

40 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients on chronic hemodialysis without significant obstructive coronary artery disease identified by angiography within one years of the study, and who had left ventricular dysfunction:

    • reduced left ventricular systolic function (left ventricular ejection fraction <55%) and/or
    • left ventricular hypertrophy evaluated by echocardiography)

Exclusion criteria

  1. Moderate or worse valvular heart disease,
  2. Past histories of acute or old myocardial infarction and/or coronary revascularization by percutaneous coronary intervention or coronary artery bypass grafting within one year of the study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Carnitine group
Experimental group
Description:
Intravenous administration of L-carnitine 1000mg after each hemodialysis session (three times a week) for one year.
Treatment:
Drug: Intravenous administration of L-carnitine
control group
No Intervention group
Description:
No intervention

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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