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Clinical Study for Yinqi Sanhuang Decoction for Detoxificationin in Treating Chronic Hepatitis B

Clinical Study for Yinqi Sanhuang Decoction for Detoxificationin in Treating Chronic Hepatitis B

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021521
Enrollment
Unknown
Registered
2019-02-25
Start date
2019-03-01
Completion date
Unknown
Last updated
2020-03-16

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

Conditions

Chronic hepatitis B

Interventions

Sponsors

Hangzhou Xixi Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients with previous history of hepatitis B or HBsAg positive for more than six months, HBsAg and/or HBV-DNA are still positive; (2) Patients who meet the antiviral indications in the guidelines or are taking entecavir dispersible tablets Patients treated with virus; (3) aged 18 to 65 years old; (4) patients with TCM syndromes of liver spleen deficiency and dampness and heat syndrome; (5) signed informed consent.

Exclusion criteria

Exclusion criteria: (1) patients with cirrhosis; (2) patients with liver cancer; (3) acute and chronic hepatitis with non-HBV hepadnavirus infection, autoimmune hepatitis, primary biliary cirrhosis, primary sclerosing cholangitis, Genetic metabolic liver disease, drug or toxic hepatitis, alcoholic liver disease; (4) pregnant or lactating women and women who plan to be pregnant during the study period; (5) those who are allergic to the test drug; (6) have mental disorders can not cooperate Patients in this study, or patients with unstable epilepsy; (7) Patients with systemic diseases such as severe heart, brain, lung, kidney, and hematopoiesis; (8) Alcoholism or other unsuitable drug test observers, or In combination with treatment, it is difficult to make a definitive evaluation of the effectiveness and safety of the drug; (9) Other circumstances that the investigator believes are not suitable for enrollment.

Design outcomes

Secondary

MeasureTime frame
HBV-DNA conversion rate;HBsAg negative rate;HBeAg serological conversion rate;liver function;Symptoms;signs;The thickness of spleen;

Primary

MeasureTime frame
Annual incidence of cirrhosis;

Countries

China

Contacts

Public ContactShourong Liu

Hangzhou Xixi Hospital

lsr85463990@126.com+86 18072930585

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 27, 2026