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Efficacy and safety of propofol tenofovir in the treatment of chronic hepatitis B complicated with chronic kidney disease: a multicenter, prospective study

Efficacy and safety of propofol tenofovir in the treatment of chronic hepatitis B complicated with chronic kidney disease: a multicenter, prospective study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100049713
Enrollment
Unknown
Registered
2021-08-08
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-04-19

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

Conditions

chronic hepatitis B

Interventions

tenofovir alafenamide group:Oral tenofovir alafenamide

Sponsors

Ningbo Huamei Hospital, University of Chinese Academy of Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Older than 18; 2.The positive time of HBsAg was more than 6 months; 3.Patients who meet the antiviral diagnosis and treatment standards in the 2019 Chinese guidelines for the diagnosis and treatment of chronic hepatitis B and have not received or are receiving oral nucleoside (acid) antiviral drugs; 4.Chronic kidney disease was diagnosed according to KDIGO guidelines in 2012. Renal injury indexes (such as proteinuria, hematuria or anatomical abnormalities) or GFR 3 months; 5.Understand and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Pregnant or lactating women; 2.With other types of hepatitis virus infection or HIV infection; 3.Patients with decompensated cirrhosis (Child B/C grade) or confirmed liver cancer or other malignant tumors; 4.Patients with glomerular filtration rate < 15 ml/min and without hemodialysis 5.Patients with mental illness

Design outcomes

Primary

MeasureTime frame
routine blood test;urinalysis;Urinary albumin / creatinine;liver function;renal function;electrolyte;Coagulation function;Hepatitis B three line quantitative analysis;Serum HBVDNA;Abdominal B-ultrasound examination;Liver transient elastic stiffness test;Bone mineral density test;

Countries

China

Contacts

Public ContactQian Yunsong

Ningbo Huamei Hospital, University of Chinese Academy of Sciences

qianyuns@163.com+86 13645740222

Outcome results

None listed

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