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Paracetamol as a tracer for plasma volume measurements: a proof of principle study.

Completed
Conditions
blood volume of the patient
plasma volume
10010273
Registration Number
NL-OMON52675
Lead Sponsor
Medisch Universitair Ziekenhuis Maastricht
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
20
Inclusion Criteria

Over 18 years of age
(pre-)eclampsia in previous pregnancy
scheduled for plasma volume measurement
agree to participate in the study

Exclusion Criteria

under the age of 18
pregnant
allergy for paracetamol
liver failure
refusal to participate in the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>Comparison of the calculated plasma volumes using paracetamol and 125I labeled<br /><br>albumin.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>not applicable</p><br>
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