Comparison of two devices for coagulation diagnostics: Multiplate® and VerifiyNOW®

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00029249

Enrollment

Registered

2022-07-21

Start date

2022-08-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

D69.58

Interventions

Group 1: Patient undergoing surgery with cardiopulmonary bypass. Blood was drawn from the patients to investigate thrombocyte function with two different point of care devices.

Eligibility

Sex/Gender

All

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Patients undergoing cardiac Surgery with use of extracorporal circulation

Exclusion criteria

Exclusion criteria: - Usage of anticogulant medication (e.g. Marcumar, DOAK) - Innate or acquired coagulation disorder - Rejection of Patient to participate in study - Pregnancy

Design outcomes

Primary

Measure	Time frame
Can the extracorporal circulation related thrombocyte dysfunction be detected by both point of care devices?	—

Countries

Germany

Contacts

Public ContactSven Oliver Schneider

Universitätsklinikum des SaarlandesKlinik für Anästhesiologie, Intensivmedizin und Schmerztherapie

Sven.Schneider@uks.eu0151 24022562

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026