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Establishment of a Nomogram model to predict portal vein thrombosis in cirrhosis and clinical study of its intervention

Establishment of a Nomogram model to predict portal vein thrombosis in cirrhosis and clinical study of its intervention

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058811
Enrollment
Unknown
Registered
2022-04-17
Start date
2022-06-01
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Cirrhosis of the liver

Interventions

Intervention group:Rifaximin (standard dose 200mg/ time, three times a day, for 14 days) + conservative treatment according to the condition
Control group:Conservative treatment according to the condition

Sponsors

The Affiliated Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-65, regardless of gender; 2. Patients with cirrhosis and PVT of cirrhosis; 3. As determined by the investigator, the subject is able to understand all relevant aspects of the study Content and comply with the requirements of the research protocol. The subject understands and signs informed consent prior to the start of the study process; 4. From signing the informed consent to the end of the study, agree to take effective contraceptive measures.

Exclusion criteria

Exclusion criteria: 1. Used antibiotics 4 weeks before treatment; 2. Primary liver cancer or other systemic tumors; 3. Liver function Child C; 4. The subject has any unstable or uncontrolled cardiovascular, pulmonary, liver, kidney, urogenital, hematological, coagulation, immunological, metabolic or other medical condition that the investigator believes would interfere with the study results or jeopardize the subject's safety; 5. The subject has a history of severe allergies; 6. Pregnant or lactating patients or patients with family planning in recent 3 months; 7. The subject has a history of substance abuse (defined as the use of any illicit drug) or alcohol abuse within 1 year prior to screening; 8. The subjects had active psychosis, which the researchers thought might interfere with their compliance with the study procedure; 9. Subject is unable to attend all study visits or follow study procedures; 10. Participated or is participating in other clinical studies within 3 months.

Design outcomes

Primary

MeasureTime frame
Rifaximin reduces the incidence of PVT in high-risk patients with cirrhosis;

Secondary

MeasureTime frame
Blood routine, endotoxin, NETs markers, liver function, blood coagulation routine and other laboratory indicators;Imaging examination for PVT;

Countries

China

Contacts

Public ContactXue Jing

The Affiliated Hospital of Qingdao University

jingxue@qdu.edu.cn+86 18661807575

Outcome results

None listed

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