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A randomized, placebo-controlled clinical study to evaluate the efficacy of Levocarnitine in the treatment of nonalcoholic fatty liver disease.

A randomized, placebo-controlled clinical study to evaluate the efficacy of Levocarnitine in the treatment of nonalcoholic fatty liver disease.

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-16008718
Enrollment
Unknown
Registered
2016-06-25
Start date
2016-06-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

nonalcoholic fatty liver disease

Interventions

treantment group:Levocarnitine 1g, bid., po., 12wks
2:no

Sponsors

Beijing Youan Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. aged 18-70 years old; 2. NAFLD patients meet the diagnosis criteria according to: The diagnosis and management of non-alcoholic fatty liver disease: practice guideline by the American Association for the Study of Liver Diseases, American College of Gastroenterology, and the American Gastroenterological Association); 3. ALT 60 to 250 U/L; 4. Patient signs an informed consent form.

Exclusion criteria

Exclusion criteria: 1) fatty liver caused by a specific cause, such as tamoxifen; 2) combined with other causes of liver disease such as viral hepatitis (such as HBsAg or anti HCV positive), liver cirrhosis, drug-induced liver injury, autoimmune diseases, metabolic liver disease, etc; 3) Alcohol abuse, alcohol consumption >70g/week for female patient or >140g/week for male patient; 4) Patient who is receiving insulin treatment; 5) patients with severe disease of other system, mental disease, or senile dementia patients, epilepsy patients; hypothyroidism or Cushing's syndrome; 6) Have received Levocarnitine treatment within 30 days; Hypersensitive to Levocarnitine and its derivatives; 7) Patient has participated in other drug clinical trial within 30 days; 8) use of drugs such as calcium channel blockers, high dose of synthetic estrogens, methotrexate, amiodarone steroids, chloroquine; 9) Pregnant or lactating female, or female of childbearing potential does not use adequate contraceptive methods; 10) other situations that researchers think the patient is not suitable for the research.

Design outcomes

Primary

MeasureTime frame
ALT level;

Secondary

MeasureTime frame
GGT;the ration of patients whose ALT decrease to normal;AST;HOMA-IR;TG;TC;HDL-C;LDL-C;Fasting blood glucose;CAP;

Countries

China mainland

Contacts

Public ContactJing Zhang

Beijing Youan Hospital, Capital Medical University

drzhangjing@163.com+86 13391859683

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026