Placental Growth Factor Assessment of Women With Suspected Pre-eclampsia
NCT02881073 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2313
Last updated 2019-08-07
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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