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Platelet Transfusion in Acute-on Chronic Liver Failure

Platelet Transfusion in Acute-on Chronic Liver Failure

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04564651
Enrollment
80
Registered
2020-09-25
Start date
2019-05-01
Completion date
2024-05-01
Last updated
2020-09-25

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

Conditions

Acute-On-Chronic Liver Failure

Brief summary

Acute on-chronic liver failure (ACLF) is a severe liver disease with a 28-day mortality rate of up to 40%. When the patients get 3 or more organ failures, the 28-day mortality rate is up to 82.6%. Though the ACLF patients have high short-term mortality, and the only effective treatment method is liver transplantation. However, few patients can be treated due to the scarcity of liver source, rapid disease progression and short transplantation window. Our team evaluated the platelet function of 100 patients with ACLF by using the thromboelastograghy (TEG 5000). It was found for the first time that the reactivity of platelets of ACLF patients decreased, and the platelet inhibition rate (especially the ADP pathway) was related to patients'short-term prognosis. When the ADP inhibition rate was 70%, the patients'28-day mortality was up to 100%. However, the mechanism of low platelet response to ADP in ACLF patients is still unclear. We found that the platelet function in patients with ACLF 2-3 grade and inhibition rate beyond 70% was improved and the 28-day mortality decreased after platelet transfusion. Whether platelet transfusion can prolong survival time needs to be determined in a prospective controlled study. Therefore, this study is expected to find a new therapeutic method to reduce the mortality of patients with ACLF.

Interventions

OTHERplatelet transfusion

when the ADP inhibition \>70%, give one unit platelet tansfusion

Sponsors

Nanfang Hospital, Southern Medical University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
16 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* 18-60 years old; * Patients with compensated cirrhosis conformed to the (ACLF) diagnostic criteria of chronic and acute liver failure defined by the European Association of Hepatology (EASL-CLIF), and met the ACLF-2 and 3 grades. ADP inhibition rate ≥ 70%.

Exclusion criteria

* Patients with severe platelet allergy in the past; * Coma caused by cerebral hemorrhage or primary diseases of the nervous system; * Those who have taken anti-platelet drugs or anticoagulants within four weeks; * Rupture and bleeding of EVB occurred within 1 week. * Those who received platelet transfusion within 1 week; * Patients with liver cancer or other malignant tumors; * Pregnant and lactating women; * Complicated with other serious chronic diseases; * Not signing the informed consent form; * Other researchers do not consider it appropriate to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
28-day transplant-free mortality28 dayswhether participant died or not without liver transplantation

Secondary

MeasureTime frameDescription
90-day transplant-free mortality90 daysmortality without transplant in 90 day

Countries

China

Contacts

Primary ContactChen Jinjun
chjj@smu.edu.cn+8618588531001
Backup ContactQi Tingting
tingtingqi@126.com+8615521287260

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026