Skip to content

Interferon treatment for chronic hepatitis B with metabolic associated fatty liver disease: a prospective, multicenter, cohort study

Interferon treatment for chronic hepatitis B with metabolic associated fatty liver disease: a prospective, multicenter, cohort study

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400084913
Enrollment
Unknown
Registered
2024-05-28
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-06-03

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

Conditions

CHB

Interventions

CHB:None
CHB and MAFLD:None

Sponsors

Beijing You 'an Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 60 Years

Inclusion criteria

Inclusion criteria: ? CHB meets the 2022 Chronic Hepatitis B Prevention and Treatment Guidelines, HBsAg positive >6 months, NA treatment, HBsAg < 1500IU/ml, HBeAg negative, HBV DNA < 10 IU/mL. ? MAFLD meets the following diagnostic criteria: liver steatosis is diagnosed by abdominal B-ultrasound or Fibroscan or hepatic adipose measurement MRI (adipose lesion is classified as mild to moderate or severe according to the threshold value of the above detection means). One of the following three conditions: 1) overweight or obese (BMI=23kg/m2); 2) Diabetes mellitus; 3) Lean/normal weight patients meet at least 2 metabolic abnormalities

Exclusion criteria

Exclusion criteria: ? Patients with HCV infection and autoimmune liver disease; ? History of heavy alcohol consumption (alcohol intake > 210g/ day for men and > 140g/ day for women); ? Secondary hepatic steatosis caused by drugs, such as tamoxifen, hormones, etc.; (4) Pregnant and lactating women and patients who are preparing to give birth in the near future; ? Patients with cirrhosis or liver cancer in the past or now; ? Other serious diseases that may affect the nutritional status of the body, such as malignant tumors, serious organic or mental diseases such as heart, lung, kidney, etc.; ? Neutrophil count 34umol/L.

Design outcomes

Primary

MeasureTime frame
48 week HBsAg clearance rate;

Secondary

MeasureTime frame
Quantitative decrease in HBsAg at 48 weeks;HBV DNA undetectable rate;HBsAg serological conversion rate;PEG-IFN adverse reactions;

Countries

China

Contacts

Public ContactCao Zhenhuan

Beijing You 'an Hospital, Capital Medical University

caozhenhuanyu@mail.ccmu.edu.cn+86 138 1024 8004

Outcome results

None listed

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