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On the Role of The (Pro)Renin-Angiotensin System in Preeclampsia

On the Role of The (Pro)Renin-Angiotensin System in Preeclampsia - RAS in preeclampsia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON32502
Enrollment
120
Registered
2009-11-26
Start date
2010-03-15
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

preeclampsia toxicosis of pregnancy

Interventions

None listed

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: pregnant women who undergo a caesarian section. women with and without preeclampsia and with or withour preexistent or gestational diabetes mellitus are included. Non-pregnant women who undergo abdominal gynaecological surgery

Exclusion criteria

Exclusion criteria: Not willing to give informed consent Use of antihypertensive medication

Design outcomes

Primary

MeasureTime frame
To assess whether concentrations of renin and prorenin in the circulation and amniotic fluid change during preeclampsia and whether circulating and amniotic fluid concentrations are inversely related. To assess whether concentrations of renin and prorenin are infuenced by diabetes mellitus. To assess the gene expression of components of the RAS, including the (pro)renin-receptor in the maternal and foetal part of the placenta and the influence of preeclampsia and diabetes mellitus. To assess the functional role of (pro)renin-receptors in the endometrium. To assess the influence of pregnancy and preeclampsia on the role of the angiotensin II, subtype 2 receptor.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)