De effecten van verschillende doseringsverhoudingen van middelen die de stolling remmen of activeren op bloedverlies tijdens hartchirurgie.

Completed

• Conditions: Cardiac surgery; coronary artery bypass graft surgery; cardiopulmonary bypass

• Registration Number: NL-OMON22454
• Lead Sponsor: VU University Medical Center

Brief Summary

/A

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 98

Inclusion Criteria

1. Patients undergoing coronary artery bypass graft (CABG) surgery;

2. Age 18-85 years;

Exclusion Criteria

1. Re-operations;

2. Emergency operation;

Study & Design

• Study Type: Interventional
• Study Design: Not specified