A Prospective Study of Application of Platelet Mapping in HBV-related Acute-on-chronic-liver Failure in China
1 other identifier
observational
100
1 country
1
Brief Summary
Ineffective hemostasis or a paradoxical prothrombotic state of Acute-on-chronic liver disease (ACLF) has been well established. Thrombelastography measures the dynamics of thrombin production and provides a global assessment of coagulation incorporating the cumulative effect of the interactions at various levels between plasma components and cellular component of coagulation. And through the platelet mapping, it can help provide a picture of patients' function of platelet. This study aims to explore the predictive role of platelet mapping in ACLF prognosis, organ failure developments and short term mortality.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Oct 2017
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 11, 2017
CompletedFirst Posted
Study publicly available on registry
September 13, 2017
CompletedStudy Start
First participant enrolled
October 30, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 13, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
August 13, 2018
CompletedJune 6, 2019
April 1, 2018
10 months
September 11, 2017
June 4, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
28-day mortality
death within 28-day
28-day
Secondary Outcomes (2)
28-day progression
28-day
90-day mortality
90-day
Interventions
standard medical treatment
Eligibility Criteria
Patients with HBV-related chronic liver disease, International Normalized Ratio (INR)≥1.5 and total bilirubin≥85μmol/L
You may qualify if:
- patient with previously diagnosed or undiagnosed HBV related chronic liver disease/cirrhosis
- INR≥1.5 and total bilirubin≥85μmol/L
You may not qualify if:
- INR≤1.5 or total bilirubin≤85μmol/L;
- underlying chronic liver disease was other than chronic HBV infection related;
- those who had hepatocellular carcinoma or other types of malignancies;
- obstructive biliary diseases or other disease lead to bilirubin evaluation;
- those who had acute hemorrhage one week before admission
- those who received platelet, cryo transfusion or plasmapheresis one week before admission
- using steroid or immunosuppressant or antiplatelet or anticoagulant drugs in 4 weeks
- any kind of decompensation which persisted over a month
- pregnancy and breastfeeding
- those who received liver transplantation or kidney transplantation;
- combine with other disease lead to organ failure including heart failure (NYHA IV),respiratory failure(PaO2\<60mmHg),renal insufficiency(CKD 5) and conscious disturbance (GCS\<8)
- readmission;
- death within 24 hours.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Nanfang Hospital
Guangzhou, Guangdong, 510515, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 11, 2017
First Posted
September 13, 2017
Study Start
October 30, 2017
Primary Completion
August 13, 2018
Study Completion
August 13, 2018
Last Updated
June 6, 2019
Record last verified: 2018-04