Paracetamol and its Influence on the Opioid Requirement in Sufficient Pain Management in the ED
- Conditions
- Opioid use, pain
- Registration Number
- NL-OMON22636
- Lead Sponsor
- Academic Medical Center (AMC), Amsterdam
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 168
Inclusion Criteria
In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- patients 18 years or older presenting to the ED in the AMC
Exclusion Criteria
A potential subject who meets any of the following criteria will be excluded from participation in this study:
- hepatic dysfunction
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The main study endpoint is the opioid requirement in Morphine Equivalent Units (MEU) between individual subjects who received additional paracetamol and those who did not.
- Secondary Outcome Measures
Name Time Method Secondary outcome is the NRS measured an hour after administration of the opioid and at discharge, between individual subjects who received additional paracetamol at the ED and those who did not.