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Clinical Trials/CTRI/2017/12/010822
CTRI/2017/12/010822
Not yet recruiting
未知

Thromboelastography guided blood product transfusion in patients undergoing invasive liver related procedures in patients with chronic liver disease: A Randomized Controlled Trial - TEG-CLD

Department of Gastroenterology AIIMS New Delhi0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: null- patients undergoing invasive liver related procedures in patients with chronic liver disease.

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- patients undergoing invasive liver related procedures in patients with chronic liver disease.
Sponsor
Department of Gastroenterology AIIMS New Delhi
Status
Not yet recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Department of Gastroenterology AIIMS New Delhi

Eligibility Criteria

Inclusion Criteria

  • •1\.Patient undergoing invasive liver related procedures (eg, percutaneous liver biopsy, transjugular liver biopsy, transarterial chemoembolization, hepatic vein angioplasty/stenting, transjugular intrahepatic portosystemic shunt (TIPS)
  • •2\.Age between 18\-65 years
  • •3\.Willing to participate in the study

Exclusion Criteria

  • •1\.Patients with malignancy/disseminated intravascular coagulation (DIC)/known coagulopathic disorder (haemophilia) apart from cirrhosis.
  • •2\.History of intake of platelets inhibitors (eg, aspirin, clopidogrel) and drugs affecting coagulation cascade (eg, vitamin K anatagonists) within past 7 days
  • •3\.Pregnant women and those on oral contraceptives
  • •4\.Patients with chronic renal failure
  • •5\.History of underlying hypercoagulable/ hypocoagulable states eg. paroxysmal nocturnal hemoglobunuria(PNH), polycythemiavera etc
  • •6\.Patients receiving blood products (fresh frozen plasma and platelet prior to thromboelastography)
  • •7\.Patients with shock
  • •9\.Not willing to provide consent.

Outcomes

Primary Outcomes

Not specified

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