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The Effect Of Dual Treatment With L-Carnitine And Magnesium On Fatty Liver

THE EFFECT OF DUAL TREATMENT WITH L-CARNITINE AND MAGNESIUM ON Patients With Non Alcoholic Fatty Liver Disease

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01956825
Enrollment
60
Registered
2013-10-08
Start date
2014-01-31
Completion date
2014-04-30
Last updated
2013-10-08

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

Conditions

Non Alcoholic Fatty Liver Disease

Keywords

non alcoholic fatty liver disease, LCARNITINE amino acid, magnesium, fat content

Brief summary

The purpose of this study is to determine whether the dual therapy of the amino acid L-CARNITINE and magnesium have an effect on reducing the liver fat content in patients with non alcoholic fatty liver disease (NAFLD).

Detailed description

The purpose of this study is to determine whether the dual therapy of the amino acid L-CARNITINE and magnesium have an effect on reducing the liver fat content in patients with non alcoholic fatty liver disease. the study is an interventional one in which 60 patients who by definition have non alcoholic fatty licer disease (NAFLD) are divided randomly (double blind) into 2 groups: group 1: study group. receive a product (flavoured water) which contains L-CARNITINE an magnesium. group 2: control. receive placebo. regular water. Length of trial - 12 weeks. The patients will be followed on a weekly base and variuos parameters will be compared (weight, lipid profile, insulin resistance etc.). fibrotest will be used at the beginning of the trial and at the end (week 12) comparing the fat content before and after the treatment.

Interventions

DIETARY_SUPPLEMENTslim water

Sponsors

Meir Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

age\>18, \<80 y evidence to non alcoholic fatty liver disease

Exclusion criteria

age\<18, \>80 y pregnancy renal failure congestive heart failure active malignancy liver disease - etiology other than non alcoholic fatty liver disease (NAFLD). hypothyroidism/cushing total prenteral nutrition (TPN) in the last 6 month

Design outcomes

Primary

MeasureTime frame
effect of LCARNITINE and magnesium treatment on the liver fat content12 weeks

Secondary

MeasureTime frameDescription
effect of L-CARNITINE and magnesium treatment on the metabolic panel12 weekshepatic enzyme profile, lipid profile, weight, inflammatory markers, insulin resistance

Countries

Israel

Contacts

Primary ContactDAN FELDMAN, MD
danifel100@gmail.com0522794025
Backup ContactYONA KITAY, MD
yonaki@clalit.org.il09-7471560

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026