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Clinical Trials/NL-OMON23031
NL-OMON23031
Completed
未知

Paracetamol as a Tracer for Plasma Volume Measurements: a Proof of Principle study

Maastricht UMC+0 sites20 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Maastricht UMC+
Enrollment
20
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational non invasive

Investigators

Eligibility Criteria

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

Outcomes

Primary Outcomes

Not specified

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