ClinicalTrials.Veeva

Menu

PREdelivery Placental Biomarkers- Pregnancy and Delivery Outcome (PREPPeD)

University of Oslo (UIO) logo

University of Oslo (UIO)

Status

Unknown

Conditions

Pregnancy Complications
Placental Insufficiency

Treatments

Other: Blood sampling

Study type

Observational

Funder types

Other

Identifiers

NCT03100084
36864
36259 (Other Identifier)

Details and patient eligibility

About

The PREPPeD study proposes that predelivery placenta-derived maternal circulating biomarkers reflect placental health, capacity and ageing, and can help predict onset and complications of delivery both in complicated pregnancies as well as in clinically uncomplicated term/post-term pregnancies.

Full description

The main aim of the PREPPeD study is to explore whether placental health, evaluated by maternal blood biomarkers in late pregnancy, correlates with delivery outcomes in both healthy and complicated pregnancies.

Enrollment

1,000 estimated patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • All pregnant women scheduled to deliver at the Department of Obstetrics at OUH who qualify for the study groups as specified in the "Groups and Intervention" section.

Exclusion criteria

  • Women who do not understand Norwegian or English
  • Communicable disease
  • Younger than 18 years of age
  • Legally incompetent
  • Fetal malformations

Trial design

1,000 participants in 7 patient groups

I. Post Dates
Description:
Pregnant women referred for clinical post term evaluation and/or labour induction. Blood sampling.
Treatment:
Other: Blood sampling
II. Induction of Labour
Description:
Pregnant women ≥37+0 GW (gestational week) referred for labour induction (any cause). Blood sampling.
Treatment:
Other: Blood sampling
III. All Outpatients
Description:
Pregnant women ≥37+0 GW presenting for any medical reason at OUH outpatient clinic. Blood sampling
Treatment:
Other: Blood sampling
IV. Diabetes in Pregnancy
Description:
Pregnant women ≥36+0 GW with pregestational or gestational diabetes. Blood sampling.
Treatment:
Other: Blood sampling
V. Reduced Fetal Movements
Description:
Pregnant women ≥37+0 GW with reduced fetal movements and/or referred due to reduced symphysis-fundal height. Blood sampling.
Treatment:
Other: Blood sampling
VI. Hypertensive Disorders in Pregnancy
Description:
Pregnant women referred for preeclampsia (or other pregnancy induced hypertensive disorders) and/or suspected fetal growth restriction; longitudinal cohorts. Blood sampling.
Treatment:
Other: Blood sampling
VII. All Labour Admissions
Description:
All pregnant women ≥37+0 GW admitted for labour. Blood sampling.
Treatment:
Other: Blood sampling

Trial contacts and locations

1

Loading...

Central trial contact

Meryam Sugulle, PhD, MD; Anne Cathrine Staff, PhD, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems