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Investigation and countermeasures of hypoviremia in chronic HBV infected patients with normal ALT after antiviral therapy

Investigation and countermeasures of hypoviremia in chronic HBV infected patients with normal ALT after antiviral therapy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092876
Enrollment
Unknown
Registered
2024-11-25
Start date
2024-11-28
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Chronic hepatitis B

Interventions

Adjust the drug according to the response to the virus: medication adjustment therapy

Sponsors

Linyi People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Age 18-65 years old, gender unlimited; 2.Patients with HBV infection who meet the diagnostic criteria of the Chronic Hepatitis B Prevention and Treatment Guidelines (2022 edition); 3.HBV DNA can be detected; 4.Patients who agree to participate in this clinical trial and voluntarily sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients younger than 18 years old and older than 65 years old ; 2. Patients co-infected with human immunodeficiency virus or requiring long-term immunosuppressants ; 3. Patients who plan to receive organ transplantation or have received organ transplantation ; 4. Patients with liver cancer or other malignant tumors; 5. Patients with serious underlying diseases, including heart, brain, lung, digestive, blood, urinary, neuropsychiatric and other diseases; 6. Patients with other liver diseases, including viral hepatitis C, alcoholic hepatitis, drug hepatitis, autoimmune liver disease, etc. 7. Have a history of alcohol or drug abuse within the last 1 year; 8. Patients who have participated in clinical trials of other drugs within the last 3 months; 9. Patients with compensatory and decompensated cirrhosis and liver failure; 10. Patients with poor compliance, unable to adhere to or unwilling to participate in the study, or patients who are not suitable to participate in the clinical study according to other researchers.

Design outcomes

Primary

MeasureTime frame
ALT;HBV DNA;Biochemical tests;

Secondary

MeasureTime frame
hepatic imaging;Blood routine examination;

Countries

China

Contacts

Public ContactXing Liu

Linyi People's Hospital

lxgjl@163.com+86 135 6298 7695

Outcome results

None listed

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