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Thromboelastometry in Assessment of Sepsis Coagulopathy

U

University Hospital, Motol

Status

Completed

Conditions

Thrombelastography
Sepsis

Study type

Observational

Funder types

Other

Identifiers

NCT02971111
1318514

Details and patient eligibility

About

The purpose of this study is to analyze occurence of bleeding complications during invasive procedures in septic patients with normal tromboelastometry results despite prolonged standard coagulation tests results

Enrollment

76 patients

Sex

All

Ages

24 to 89 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • sepsis/septic shock
  • prolonged PT-INR (international normalized ratio) ≥ 1.3
  • normal ROTEM-EXTEM results.

Exclusion criteria

  • patients on antiplatelet drugs or anticoagulant therapy (heparin, vitamin K antagonists...)
  • patients with cirrhosis

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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