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Assessment of Hemostatic Profile in Liver Cirrhosis

G

Goethe University

Status

Completed

Conditions

Coagulation Disorder

Treatments

Other: Assessment of hemostatic profile

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Our study included both in- and outpatients suffering from liver cirrhosis attending the out- and inpatient care of the department of hepatology. Demographic and biochemical data as well as medical history including cause of liver cirrhosis, end stage kidney failure and medication with anticoagulants were recorded. To assess the hemostatic profile, platelet function was analyzed by multiple electrode aggregometry (MEA) using Multiplate (ADP-, ASPI- and TRAP-test) and thrombelastometry using ROTEM (EXTEM, INTEM, FIBTEM).

Enrollment

67 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • liver cirrhosis
  • age of ≥ 18 years
  • platelet count of at least 70 / nl

Exclusion criteria

  • transfusion of platelet concentrate three weeks prior to inclusion
  • pregnancy
  • age < 18 years
  • missing informed consent

Trial design

67 participants in 2 patient groups

Low MELD score
Description:
MELD score of 6 - 11
Treatment:
Other: Assessment of hemostatic profile
High MELD score
Description:
MELD score of ≥ 17
Treatment:
Other: Assessment of hemostatic profile

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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