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Clinical evaluation on activation of coagulation and fibrinolytic system during major cardiovascular surgery

Clinical evaluation on activation of coagulation and fibrinolytic system during major cardiovascular surgery - Clinical evaluation on activation of coagulation and fibrinolytic system during major cardiovascular surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000010866
Enrollment
60
Registered
2013-06-17
Start date
2013-04-14
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

major cardiovascular surgery with use of cardiopulmonary bypass

Interventions

None listed

Sponsors

Teikyo University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: aortic replacement surgery,other cardiovascular surgery,re-surgery for cardiovascular replacement

Exclusion criteria

Exclusion criteria: patients with congenital bleeding diathesis, patients with thrombocytopenia less than 100,000/uL continuing more than one month, patients with taking oral anticoagulant/antiplatelet agents

Design outcomes

Primary

MeasureTime frame
activated factor VII, thrombin-antithrombin complex (TAT), fibrin monomer, fibrin degradation product (FDP), D-dimer, plasmin-plasmin inhibitor complex (PIC), fibrinogen, PT, APTT, platelet count, hemoglobin, from just before the start of cardiopulmonary bypass until entrance into the intensive care unit

Countries

Japan

Contacts

Public ContactSATO HIDEO

Teikyo University Hospital anesthesiology

hideos3150@yahoo.co.jp03-3964-1211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026