Thromboelastometry in Assessment of Sepsis Coagulopathy

NCT02971111 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 76

Last updated 2018-09-10

No results posted yet for this study

Summary

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

Conditions

Sponsors & Collaborators

  • Charles University, Czech Republic

    collaborator OTHER
  • University Hospital, Motol

    lead OTHER

Eligibility

Min Age
24 Years
Max Age
89 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2016-10-31
Completion
2016-10-31

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02971111 on ClinicalTrials.gov