Cirrhosis, Liver Clinical Trial
Official title:
Clinical Validation of the Use of Global Coagulation Tests Like Thromboelastography and Sonoclot in Liver Disease - A Prospective Observational Study.
NCT number | NCT04332484 |
Other study ID # | 586 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | January 1, 2018 |
Est. completion date | August 31, 2019 |
Verified date | April 2020 |
Source | Postgraduate Institute of Medical Education and Research |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Background: Patients with cirrhosis and acute-on-chronic liver failure (ACLF) may have
bleeding complications which can lead to increased mortality. Standard coagulation tests
(SCTs) like prothrombin time, platelet count and activated partial thromboplastin do not
accurately depict in vivo coagulation profile. Point-of-care viscoelastic coagulation testing
devices like thrombo-elastography (TEG) and Sonoclot may be better for guiding patient
management.
Methods: This prospective observational study compared and validated the point of care (POC)
tests and SCTs in 70, 72 and 25 persons with ACLF, decompensated cirrhosis and healthy
controls respectively.
Status | Completed |
Enrollment | 142 |
Est. completion date | August 31, 2019 |
Est. primary completion date | August 31, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - All patients with Acute on Chronic Liver Failure - All patients with cirrhosis of Liver Exclusion Criteria: - Recent blood or blood component transfusion in last 2 weeks - HIV infection - Antiplatelet, anticoagulant or antifibrinolytic therapy - Patients on Dialysis - Pregnant females - Active malignancy in last 5 years - Chronic heart failure - Chronic pulmonary disease - End stage renal disease |
Country | Name | City | State |
---|---|---|---|
India | PGIMER | Chandigarh |
Lead Sponsor | Collaborator |
---|---|
Postgraduate Institute of Medical Education and Research |
India,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Validation of TEG and Sonoclot | To clinically validate the comparibility of results obtained from the TEG and Sonoclot instruments | Day 3 | |
Secondary | Correlation of Point of care test with standard coagulation tests | To investigate whether variables from TEG or Sonoclot analyses correlated with Standard Coagulation Tests | Day 3 | |
Secondary | Correlation of Point of care tests with bleeding event | To assess whether a coagulation defect on TEG or Sonoclot predicts a bleeding event or not. | Day 28 | |
Secondary | Correlation of Point of care tests with mortality | To assess whether a coagulation defect on TEG or Sonoclot predicts mortality | 28 days |
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