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Study of thromboelastography characteristics in patients with liver cirrhosis andits application in guiding clinical plasma transfusion

Study of thromboelastography characteristics in patients with liver cirrhosis andits application in guiding clinical plasma transfusion

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15007174
Enrollment
Unknown
Registered
2015-10-07
Start date
2016-06-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Liver cirrhosis

Interventions

healthy control:coagulation tests
patients admitted with liver cirrhosis:coagulation tests
patients guided by conventional coagulation tests:plasma transfusion guided by conventional coagulation tests
patients guided by TEG:plasma transfusion guided by TEG

Sponsors

Department of Blood Transfusion, Daping Hospital, Research Institute of Surgery, Third Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 79 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 79 years old; 2. patients admitted to Digestive Department with a diagnosis of liver cirrhosis; 3. Patients who are willing to participate in the study with informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients who are unable to communicate due to a history of stroke, epilepsy, or primary brain cancer patients, cancer patients with brain metastases; 2. cirrhosis patients with hepatocellular carcinoma; 3. patients with liver dysfunction or liver failure; 4. patients who have taken medicines that may affect the coagulation function(like heparin, coumarin anticoagulants andthrombin inhibitors); 5. patients who have serious organic disease in heart, lung or kidney; 6. pregnant or lactating women; 7. patients who are involved in another clinical research; 8. patients who refuse to participate in the research; 9. patients who took part in other clinical drug test in 3 month before being enrolled in our study; 10. other situations.

Design outcomes

Primary

MeasureTime frame
TEG characteristics in different Child-Pugh class cirrhosis patients;evaluation standard of TEG by different Child-Pugh class;

Countries

China

Contacts

Public ContactWen Aiqing
dpyysxkwaq@hotmail.com+86 023-68757651

Outcome results

None listed

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