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A multicenter clinical study of propofol tenofovir fumarate in the treatment of DNA positive hepatitis B carriers

A multicenter clinical study of propofol tenofovir fumarate in the treatment of DNA positive hepatitis B carriers

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200060940
Enrollment
Unknown
Registered
2022-06-14
Start date
2022-06-01
Completion date
Unknown
Last updated
2023-03-26

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

Conditions

HBV

Interventions

Test Group:Take TAF orally
matched group:Take TDF orally

Sponsors

Affiliated Hangzhou First People’s Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Hepatitis B surface antigen positive, and HEPATITIS B VIRUS DNA positive, but no liver cirrhosis, liver cancer, no HEPATITIS B virus carriers with elevated ALT; 2) 18-75 years old; 3) Understand and sign informed consent.

Exclusion criteria

Exclusion criteria: 1) With other types of hepatitis virus or HIV infection; 2) Participated in other clinical trials in recent 1 month; 3) Women who are pregnant or breastfeeding; 4) Simultaneous use of other antiviral drugs; 5) History of schistosomiasis cirrhosis; 6) intrahepatic cholangiolithiasis with cholangitis; 7) Patients with severe fatty liver; 8) Patients with various autoimmune liver diseases; 9) Allergic history of TAF, TDF and its components; 10) acute and chronic renal insufficiency;

Design outcomes

Primary

MeasureTime frame
Liver stiffness;

Secondary

MeasureTime frame
blood routine examination;hepatorenal function;Liver fibrosis index 5;HBV DNA;Liver CT/MR;

Countries

China

Contacts

Public ContactXu Xiao
zjxu@zju.edu.cn13588191177

Outcome results

None listed

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