Clinical decision-support with Viscoelastic Haemostatic Assay; towards a more practical guided and proactive use of clotting agents

Recruiting

• Conditions: Coagulation; haemorrhage; 10007593

• Registration Number: NL-OMON50862
• Lead Sponsor: Intensive Care

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: Not specified
• Target Recruitment: 500

Inclusion Criteria

>= 18 years of age
Planned for cardiac on-pump surgery
Informed consent

Exclusion Criteria

- Failed blood sample collection
- No on-pump procedure

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>The primary objective of this study is to provide a guideline model through VHA<br /><br>analysis for optimal coagulation management in the OR and/or ICU to reduce<br /><br>blood loss. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Patient specific data like demographic information and intermittently recorded<br /><br>pre- intra and postoperative data, will be collected.</p><br>