Placental Growth Factor Assessment of Women With Suspected Pre-eclampsia

NCT02881073 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2313

Last updated 2019-08-07

No results posted yet for this study

Summary

The primary aim is to establish the effectiveness of plasma PlGF measurement in reducing maternal morbidity (with assessment of perinatal safety in parallel) in women presenting with suspected pre-eclampsia prior to 37 weeks' gestation.

The long term aim is to demonstrate that knowledge of PlGF measurement enables appropriate stratification of the antenatal management of women presenting with suspected pre-eclampsia, such that those at highest risk receive greater surveillance with a decrease in maternal adverse outcomes, and those at lower risk can be managed without unnecessary admission and other interventions, such that the results would influence international clinical practice in antenatal patient healthcare

Conditions

  • Pre-eclampsia
  • Pregnancy, High Risk
  • Pregnancy Complications

Interventions

OTHER

Maternal plasma PlGF quantification

A point of care test performed on maternal plasma, to quantify the level of the protein PlGF (placental growth factor) in the serum of the pregnant woman with suspected pre eclampsia to help the clinician in stratifying the level of further care for her in her pregnancy

Sponsors & Collaborators

  • National Maternity Hospital, Ireland

    collaborator OTHER
  • Rotunda Maternity Hospital, Dublin

    collaborator UNKNOWN
  • Coombe Women and Infants University Hospital

    collaborator OTHER
  • University College Hospital Galway

    collaborator OTHER
  • Royal Jubilee Maternity Hospital, Belfast

    collaborator UNKNOWN
  • Cork University Maternity Hospital

    collaborator OTHER
  • Univerisy Maternity Hospital, Limerick

    collaborator UNKNOWN
  • University College Cork

    collaborator OTHER
  • Irish Centre for Fetal and Neonatal Translational Research

    lead OTHER

Principal Investigators

  • Louise C Kenny, PhD, MD · Irish Centre for Fetal and Neonatal Translational Research

Study Design

Allocation
RANDOMIZED
Purpose
DIAGNOSTIC
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-06-29
Primary Completion
2019-04-26
Completion
2019-04-26

Countries

  • Ireland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02881073 on ClinicalTrials.gov