Comparison of the Diagnosis Time of VET and SCL in Patients With Intraoperative Coagulopathy

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age19+
SponsorKonkuk University Medical Center

About this trial

The present study is a prospective, multi-center observational trial comparing the times taken to diagnose coagulopathies using point-of-care (POC) viscoelastic tests or standard central laboratory tests (SCL tests) in patients with intraoperative bleeding.

Eligibility criteria

Qualifiers

patients who will undergo elective surgery with a high risk of moderate to severe amount of intraoperative bleeding or coagulopathy (e.g., cardiac surgery, joint replacement, spine surgery, hepatectomy, radical prostatectomy)

patients who provide written informed consent

patients who may warrant the intraoperative use of POC viscoelastic test or SCL test

Disqualifiers

pregnancy

withdrawal of consent

termination of surgery without performing either POC viscoelastic test or SCL tests

when the study conductor deems it inappropriate to proceed with the protocol with the patient

Trial design

Treatments tested in this trial

  • SCL tests
  • POC viscoelastic tests

Treatment groups

210 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Konkuk University Medical Center

Lead sponsor

Korea Health Industry Development Institute

Collaborator

Asan Medical Center

Collaborator

Samsung Medical Center

Collaborator

Soon Chun Hyang University

Collaborator