A pharmacokinetic study of intravenous paracetamol in patients after cardiac surgery

Completed

• Conditions: post-operative pain; 10007593

• Registration Number: NL-OMON30132
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 18 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 12

Inclusion Criteria

patients scheduled for elective cardio-surgery
over 18 years of age
able and willing to consent

Exclusion Criteria

clinically significant hepatic dysfunction, body weight above 100 kg, known hypersensitivity to paracetamol or pregnancy

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Paracetamol concentrations</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>None</p><br>