Paracetamol as a Tracer for Plasma Volume Measurements: a Proof of Principle study
Not Applicable
Completed
- Conditions
- <p>(pre-)eclampsia</p>10029903
- Registration Number
- NL-OMON23031
- Lead Sponsor
- Maastricht UMC+
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
women of at least 18 years of age, (pre-)eclampsia in prior pregnancy, scheduled for PV measurement, agree to participate in the study
Exclusion Criteria
under the age of 18, pregnant, allergy for paracetamol, known to have liver disease which impairs the metabolism of paracetamol, acute liver failure, refusal to participate in the study
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>determination if paracetamol can be used effectively and accurately in determining PV as compared to the gold standard</p><br>
- Secondary Outcome Measures
Name Time Method <p>not applicable</p><br>