Comparative Analysis of PCM With ROTEM in the Measurement of Viscoelastic Coagulation Parameters

Status unconfirmed

Conditions studied: Hemostasis Monitoring

In brief

To determine if PMC viscoelastic coagulation parameters correlate with those generated by a marketed device in adult patients who require hemostasis monitoring or who are at risk of bleeding or thrombotic indications

Key facts

Study ID

NCT03679286

Run by

Entegrion, Inc.

People needed

120

Starts

2018-08-20

Expected to finish

2021-03-31

Last updated by the study team

2020-04-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age 18 years or older
• In opinion of investigator, absence of anything that precludes subject from being good study candidate
• Informed consent
• Order for measurement of hemostasis status of patients who are at risk for being hyper-coagulable or hypo-coagulable due to clinical diagnosis or medical need

You may not qualify if…

• Previous enrollment in study
• Incarcerated
• Heparin infusion in prior 24 hours

Where it is running

• Washington University in St. Louis — St Louis, Missouri, United States (enrolling)
• Thomas Jefferson University — Philadelphia, Pennsylvania, United States (enrolling)
• Ohio State University — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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