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Evaluation of Clinical Efficacy of Tiaoganhuazhuo Decoction Combined with Exercise Therapy on MAFLD Based on Magnetic Resonance Imaging

Evaluation of Clinical Efficacy of Tiaoganhuazhuo Decoction Combined with Exercise Therapy on MAFLD Based on Magnetic Resonance Imaging

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2022000065
Enrollment
Unknown
Registered
2022-06-27
Start date
2022-09-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

metabolic associated fatty liver disease

Interventions

one:Tiaoganhuazhuo Decoction Combined with Exercise Therapy
two:Tiaoganhuazhuo Decoction

Sponsors

Guang'anmen Hospital,CHINA ACADEMY OF CHINESE MEDICAL SCIENCE
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: ? Conform to MAFLD's western medicine diagnostic criteria and TCM syndrome diagnostic criteria; ? Aged between 18 and 65; ? Those who have good compliance, are willing to cooperate with the treatment, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: ? Pregnant or lactating women; ? Complicated with serious diseases of important organs (such as heart, brain, lung and kidney); ? Patients with infectious hepatitis and liver cirrhosis and liver cancer diagnosed by liver biopsy; Or drug-induced liver disease, genetic factors and other specific diseases that can lead to fatty liver; ? Patients with mental and legal disabilities; ? Suspected or actual history of drug abuse; Alcohol consumption history > 5 years, equivalent to alcohol consumption = 40 g /d for men and = 20 g /d for women; Or have a history of heavy drinking within 2 weeks, equivalent to alcohol volume > 80 g /d; ? Those who are known to be allergic to the components of the drug; ? MRI and exercise contraindications; ? Patients who are participating in other drug clinical trials or who have participated in drug clinical trials within the past month.

Design outcomes

Primary

MeasureTime frame
MRI-PDFF;

Secondary

MeasureTime frame
Liver function test;the waist;glycosylated hemoglobin;Hypersensitive C-reactive protein;TCM symptom score;Blood lipid test;uric acid;routine blood test;Fasting blood glucose;Body mass index;

Countries

People's Republic of China

Contacts

Public ContactXiaping Tao
taoxiaping@163.com15611085848

Outcome results

None listed

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