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More info
You can access this
clinical trial
if you have
Pre-eclampsia, Pregnancy, High Risk or Pregnancy Complications
and you are
over 18
years old
-
The phase for this study is not defined.
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The purpose

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

Provided treatments

  • Other: Maternal plasma PlGF quantification

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT02881073. The sponsor of the trial is Irish Centre for Fetal and Neonatal Translational Research and it is looking for 2313 volunteers for the current phase.
Official trial title:
PARROT Ireland: Placental Growth Factor in Assessment of Women With Suspected Pre-eclampsia to Reduce Maternal Morbidity: a Randomised Control Trial