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NIfedipine levels in Mothers with and without PreEclampsia and their Newborns.

NIfedipine levels in Mothers with and without PreEclampsia and their Newborns. - NIMPEN

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON46737
Enrollment
48
Registered
2018-09-28
Start date
2019-03-07
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

for instance preeclampsia hypertensive pregnancy disorders

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - pregnant - prescription of nifedipine - delivery planned in Sophia Children*s hospital - understanding of Dutch / English in speaking and reading - written informed consent

Exclusion criteria

Exclusion criteria: - not unwilling or unable to give written informed consent - multiple pregnancy - infectious diseases (e.g. HIV, hepatitis B, ZIKA) for laboratory safety - fetal congenital abnormalities - manual placenta removal

Design outcomes

Primary

MeasureTime frame
Concordance between the fetal/maternal ratio (both predicted and calculated) between pregnancies without and with hypertension or PE. Since variation is expected to be high, values 1 (fetal accumulation) will be considered as similar between both groups.

Secondary

MeasureTime frame
Concordance between the fetal/maternal ratio between the placental perfusion model and the in vivo data. Since variation is expected to be high, values 1 (fetal accumulation) will be considered as similar between both groups.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)