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Peroperatieve researchstudy with de ROTEM machine to hemostase of patients during aorta abdominalis aneurysm operation.

Peroperatieve researchstudy with de ROTEM machine to hemostase of patients during aorta abdominalis aneurysm operation. - ROTEM study

Status
Unknown
Phases
Phase 4
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON37252
Enrollment
40
Registered
2013-10-31
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Haemostasis

Interventions

None listed

Sponsors

Maasstadziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: aneurysm aorta abdominalis

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

MeasureTime frame
Correlation between ROTEM and clotting parameters values, blood loss and bloedtransfusie—

Secondary

MeasureTime frame
IC recording, infections, ventilatory and circulatory support—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)