Diagnosis of pre-eclampsia.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON20514

Enrollment

Registered

2010-09-20

Start date

2010-11-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

pre-eclampsia

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: Case: Pregant women with suspected pre-eclampsia. Control: Pregnant women admitted for a primary C. section.

Exclusion criteria

Exclusion criteria: Case: 1. Pre-existing hypertension. Control: 1. Presence of contractions; 2. Pre-existing hypertension.

Design outcomes

Primary

Measure	Time frame
Difference between pregnant women with and without pre-eclampsia for the biomarkers sFlt-1, PlGf and ratio.	—

Secondary

Measure	Time frame
1. Is the value of sFlt-1, PlGf and ratio a prognostic measure to assess severity of the disease? 2. Can these markers be used to make a desiscion on management of the pregnant women (estrictive vs. proactive).	—

Contacts

Public ContactM.T.M. Raijmakers

PO Box 4446

mraijmakers@atriummc.nl+31 (0)45 5766340

Outcome results