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Efficacy and safety of anticoagulant therapy for chronic liver disease complicated with COVID-19

Efficacy and safety of anticoagulant therapy for chronic liver disease complicated with COVID-19

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300067855
Enrollment
Unknown
Registered
2023-01-29
Start date
2023-02-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

novel coronavirus pneumonia,chronic liver disease

Interventions

The anticoagulant group was used:N/A
No anticoagulant drugs were used:N/A

Sponsors

The Third Hosptial of Zhenjiang Affiliated Jiangsu University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 100 Years

Inclusion criteria

Inclusion criteria: 1. No age limitation, no gender limitation; 2. Diagnostic criteria: Diagnostic criteria for patients with novel coronavirus infection Reference: Diagnosis and treatment Protocol for novel coronavirus infection (trial version 10) : (1) Clinical manifestations related to COVID-19 infection; (2) Have one or more of the following etiological and serological test results: 1) COVID-19 nucleic acid test is positive; 2) Test positive for COVID-19 antigen; 3) Isolation and culture of the novel coronavirus are positive; 4) The level of novel coronavirus specific IgG antibody increased 4 times or more in the convalescent phase than in the acute phase. 3. Patients with chronic liver disease, such as chronic hepatitis B (CHB), alcoholic fatty liver disease (AFID), non-alcoholic fatty liver disease (NAFID), primary biliary cirrhosis (PBC), primary sclerosing cholangitis (PSC), autoimmune hepatitis (AIH), cirrhosis, liver cancer, etc. Diagnostic criteria refer to the guidelines for specific diseases.

Exclusion criteria

Exclusion criteria: Any one of the following is not eligible: 1. Incomplete clinical data; 2. Patients with mental disorders and other serious diseases; 3. Withdrawal and lost visitors.

Design outcomes

Primary

MeasureTime frame
D-dimer;PT;APTT;fibrinogen;INR;ALT;AST;ALP;WBC;PLT;Hb;B ultrasound;Chest and abdominal CT;

Countries

China

Contacts

Public ContactTan Youwen

The Third Hosptial of Zhenjiang Affiliated Jiangsu University

tyw915@sina.com+86 13914567088

Outcome results

None listed

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