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NCT06115122Recruiting

PEPPI Study: Identification of Women at Risk for Placental Dysfunction

PEPPI Study: Identification of Women at Risk for Placental Dysfunction During the First and Third Trimesters of Pregnancy

Source: ClinicalTrials.gov · Last updated 5 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

The main purpose of this study is to evaluate Fetal Medicine Foundation's pre-eclampsia risk calculator using maternal characteristics, first trimester serum placental growth factor (PlGF) and mean arterial pressure (MAP) in a Finnish general population. Condition or disease: pre-eclampsia, intrauterine growth restriction, polycystic ovary syndrome

Status (registry)
Recruiting
Study type
Observational
Enrollment
3000 (estimated)
First submitted
28 Nov 2022
Start date
Feb 2022
Primary completion date
Dec 2027
Lead sponsor
Oulu University Hospital
NCT number
NCT06115122

What you commit to

  • Study type: Observational
  • Planned participants: 3000
  • From Feb 2022 to the primary completion date, Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Multiple pregnancy
  • Miscarriage/termination of the index pregnancy
  • No first trimester blood sampling
  • No first or third trimester blood sampling
  • No umbilical cord blood sample after baby is born
    • Fathers
  • Does not understand Finnish
    • Children
  • No consent from parent(s)
  • Mother/father declines participation
  • No consent from parent(s)
  • No blood samples from mother
  • No blood samples from child

Who the study is looking for

  • Pregnant (first trimester)
  • Understands Finnish
  • ≥18 years
  • Signed informed consent
  • Participates in PEPPI-study (criteria above)
  • Blood samples at first and third trimester of pregnancy
  • Permits blood sampling from the umbilical cord when the baby is born
  • Biological father to the child born for the mother who participated in PEPPI study
  • ≥18 years
  • Signed informed consent
  • Born to mother who participated in PEPPI study
  • Signed informed consent from parent(s)
  • Signed informed consent from parent(s)
  • Mother has blood samples taken at first and third trimester (iron status)
  • Child has blood samples taken at birth and at 3 months of age

Criteria the registry did not label

  • Mothers

Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The Wellbeing Services County of North Ostrobothnia
Coordinator of this site? Confirm its status
OuluFinlandRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.