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Clinical Trials/NCT02322697
NCT02322697CompletedNot Applicable

Effects of Chronic Intravenous Administration of L-carnitine on Myocardial Fatty Acid Metabolism in Hemodialysis Patients

Toujinkai Hospital0 sites60 target enrollmentStarted: August 2013Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
60
Primary Endpoint
changes in BMIPP summed scores of the SPECT imaging

Study Overview

Brief Summary

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.

Detailed 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
40 Years to 85 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

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

  • Moderate or worse valvular heart disease,
  • 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.

Arms & Interventions

Carnitine group

Experimental

Intravenous administration of L-carnitine 1000mg after each hemodialysis session (three times a week) for one year.

Intervention: Intravenous administration of L-carnitine (Drug)

Outcomes

Primary Outcomes

changes in BMIPP summed scores of the SPECT imaging

Time Frame: one year: September 2013-October 2014 (up to 2 years)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Toujinkai Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Masato Nishimura, MD

Director of cardiovascular division

Toujinkai Hospital

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