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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04718051
Other study ID # N202007032
Secondary ID
Status Recruiting
Phase Phase 4
First received
Last updated
Start date January 13, 2021
Est. completion date December 31, 2021

Study information

Verified date December 2020
Source Taipei Medical University WanFang Hospital
Contact Ming Shun Wu, PHD
Phone +886229307930
Email vw1017@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

With the Westernization of the diet and insufficient exercise, Taiwan's population of obesity, diabetes, and hyperlipidemia has increased in recent years, and the prevalence of the non-alcoholic fatty liver disease has gradually increased. Although weight loss, dietary adjustments, and certain drug treatments can delay the deterioration of the disease; however, weight loss and dietary adjustment are not easy.


Description:

With the Westernization of the diet and insufficient exercise, Taiwan's population of obesity, diabetes, and hyperlipidemia has increased in recent years, and the prevalence of the non-alcoholic fatty liver disease has gradually increased. Although weight loss, dietary adjustments, and certain drug treatments can delay the deterioration of the disease; however, weight loss and dietary adjustment are not easy. Moreover, drugs also have side effects, and there is currently no convenient and effective treatment for people who have non-alcoholic fatty liver disease. The purpose of this trial is that investigating and evaluating the effects on fatty liver, liver fiber, and metabolic indexes after subjects using Shen Pu Yang Gan Wan.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 31, 2021
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group 35 Years to 75 Years
Eligibility Inclusion Criteria: - Patients with fatty liver diagnosed by abdominal ultrasound or hepatic fibrometer within half a year's data - Subjects with the non-alcoholic fatty liver disease - The severity of fatty liver should be at least 3 points by taking an abdominal ultrasound Exclusion Criteria: - Female patients are pregnant or breastfeeding. - Patients with viral hepatitis. - Long-term drinkers. - Those who use slimming products and vitamin E.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Shen Pu Yang Gan Wan
Shen Pu Yang Gan Wan is Traditional Chinese Medicine; in addition, it has a high dose.
Placebo
Shen Pu Yang Gan Wan is Traditional Chinese Medicine; however, it has a very low dose.

Locations

Country Name City State
Taiwan Wanfang Hospital Taipei Wenshan District

Sponsors (2)

Lead Sponsor Collaborator
Taipei Medical University WanFang Hospital Sheng Pu Pharmaceutics Co., Ltd.

Country where clinical trial is conducted

Taiwan, 

References & Publications (1)

Yang MD, Chiang YM, Higashiyama R, Asahina K, Mann DA, Mann J, Wang CC, Tsukamoto H. Rosmarinic acid and baicalin epigenetically derepress peroxisomal proliferator-activated receptor ? in hepatic stellate cells for their antifibrotic effect. Hepatology. 2012 Apr;55(4):1271-81. doi: 10.1002/hep.24792. Epub 2012 Mar 1. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Change in AST index Measure the changes in the index which is AST relate to Liver inflammation 36 weeks
Primary Change in ACT index Measure the changes in the index which is ACT relate to Liver inflammation 36 weeks
Primary Change in HbA1c Measure the changes in the index which is HbA1c relate to Liver inflammation 36 weeks
Primary Fibroscan Measure the changes in the index which is Liver Fibrosis 36 weeks
Secondary Measuring Body Mass Index Measuring Body Mass Index (BMI). Measure the changes in index which is Metabolism 36 weeks
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