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Hepatokines and platelet aggregation function level changes in patients with cirrhosis: a case-control study

Hepatokines and platelet aggregation function level changes in patients with cirrhosis: a case-control study

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000031953
Enrollment
Unknown
Registered
2020-04-16
Start date
2020-04-01
Completion date
Unknown
Last updated
2020-04-20

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

Conditions

Liver cirrhosis

Interventions

Cirrhosis group:N/A
CHB group:N/A

Sponsors

The Third Affiliated Hospital of Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18-70 years; 2. Patients were diagnosed liver cirrhosis by clinical, biochemical, imaging or pathological examination, the diagnostic criteria are in accordance with the "Guideline for Diagnosis and Treatment of Cirrhosis; 3. According to the guidelines of diagnostic criteria for chronic hepatitis b (2019 edition), those who meet HBsAg or (and) HBV DNA positive for more than 6 months, and show liver fibrosis or elevated liver enzymes caused by continuous infection of hepatitis B virus; 4. Healthy control group: physical examination report must include blood routine, liver function, biochemistry, blood lipids, preoperative screening, in which no obvious abnormalities are found; abdominal color ultrasound without fatty liver / liver fibrosis; no systemic disease; no platelet inhibitor, non steroidal anti-inflammatory drugs, LMWH or warfarin were taken in the past 14 days; 5. Signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Women in pregnancy; 2. Active bleeding, platelet transfusion, or use of platelet inhibitor, non steroidal anti-inflammatory drugs, LMWH or warfarin in the past 14 days; 3. A history of malignant tumors, uremia, rheumatic diseases that may affect coagulation function, or other obvious metabolic abnormalities.

Design outcomes

Primary

MeasureTime frame
platelet aggregation;FGF21, RBP4;

Countries

China

Contacts

Public ContactXiuqing Wei

The Third Affiliated Hospital of Sun Yat-Sen University

weixq@mail.sysu.edu.cn+86 20-85253082

Outcome results

None listed

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