Validation of 2 different devices for activated coagulation time in cardiac surgery with cardiopulmonary bypass

Validation of 2 different devices for activated coagulation time in cardiac surgery with cardiopulmonary bypass - Validation of 2 different devices for activated coagulation time in cardiac surgery with cardiopulmonary bypass

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000031225

Enrollment

Registered

2018-02-11

Start date

2018-02-15

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

Cardiac Surgeries with cardiopulmonary bypass

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients over 20 years of age who undergo cardiac surgery with cardiopulmonary bypass

Exclusion criteria

Exclusion criteria: Shock patients

Design outcomes

Primary

Measure	Time frame
Differences in activated coagulation time between 2 different devices for activated coagulation time	—

Countries

Japan

Contacts

Public ContactMasayuki Shibasaki

Kyoto Prefectural University of Medicine Department of Anesthesiology

mshiba@koto.kpu-m.ac.jp075-251-5633

Outcome results