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

Phase 4

Withdrawn

• Conditions: Haemostasis; 10064477

• Registration Number: NL-OMON37252
• Lead Sponsor: Maasstadziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Withdrawn
• Sex: Not specified
• Target Recruitment: 40

Inclusion Criteria

aneurysm aorta abdominalis

Exclusion Criteria

None

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Correlation between ROTEM and clotting parameters values, blood loss and<br /><br>bloedtransfusie</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>IC recording, infections, ventilatory and circulatory support</p><br>