A Point-of-care Electrochemical-based Device for Rapid Detection of Fibrinogen on Type A Aortic Dissection Surgery

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

About this trial

This study compares the results of the existing fibrinogen concentration monitoring technology to the Electrochemical-based device, a point-of-care and rapid method,using a small amount of extra blood obtained in Type A Aortic Dissection Surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Participants for this study will be recruited at the Second Affiliated Hospital Zhejiang University School of Medicine. For part 1:The study participants will be adult underwent routine hemostasis analysis. For part 2:The study participants will be adult underwent surgery for acute type A aortic dissection and requires routine TEG test, residual blood samples collected for fibrinogen detection by the Clauss method and electrochemical method.

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • the Electrochemical-based device

    Diagnostic test

    Electrochemical-based device for rapid detection of fibrinogen is a novel POC diagnostic method, which is suitable for operating theatres and emergency rooms.

Treatment groups

150 Participants
are divided into 1 treatment group
Group A: The patients undergoing routine coagulation tests1 intervention

Trial outcomes

Primary outcomes

1

The fibrinogen concentration values obtained using the Clauss method and electrochemical method were compared

Time frame
1 day

Secondary outcomes

1

the time of the two detection methods

Time frame
1 day

Other outcomes

Sponsors and contacts

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