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Evaluation the effects of L Carnitine on quality of life of the cirrhotic patients

Phase 3
Recruiting
Conditions
iver cirrhosis.
Cirrhosis of the liver
K70, K74
Registration Number
IRCT20180313039075N1
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
120
Inclusion Criteria

Cirrhotic patients who referred to Liver clinic of Taleghani hospital withage 18-70 years old
Cirrhotic patients who referred to Liver clinic of Taleghani hospital with known case of cirrhosis
Cirrhotic patients who referred to Liver clinic of Taleghani hospital with Child score A or B
Cirrhotic patients who referred to Liver clinic of Taleghani hospital with no administration of L-Carnitine before

Exclusion Criteria

Not tolerate use of L-Carnitine because of the gastrointestinal problem
Gastrointestinal bleeding
Uncontrolled malignant tumors
Need of hemodialysis
Pregnancy
Receiving drugs causing hyperammonemia
Overt hepatic encephalopathy
Patients who do not accept to continue the study
Patients with other significant background diseases (heart failure, chronic kidney disease,…)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Quality of life. Timepoint: First, 3 months later, 6 months later. Method of measurement: Standard questionnaire for quality life in cirrhotic patients.;Sarcopenia. Timepoint: First, 3 months later, 6 months later. Method of measurement: Evaluate gripe strength by dynamometer and muscle mass by bioelectrical impedance analysis (BIA).
Secondary Outcome Measures
NameTimeMethod
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