Skip to main content
OpenTrials
Completed

NCT Number: NCT03284528

Does Placenta Pathology Predict Outcome of Neonates With Hypoxic Ischemic Encephalopathy?"

The histology of the placenta of newborn infants with perinatal asphyxia and hypoxic-ischaemic encephalopathy is analysed. There will be an evaluation if placenta could be a biomarker for neurodevelopmental outcome at 18-24 months of age.

Completed

Looking for future studies?

Notify Me

Key information

Age range

1 day–4 day

Sex eligibility

All sexes

Study type

Observational

Primary location

University Children's hospital Zurich

Zurich, 8044, Switzerland

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

all newborn infants with APGAR <5 at 10minutes, pH<7.0, lactate >12mmol/L, base excess >16, resuscitation >10min after birth, gestational age >35 weeks and an encephalopathy -

Exclusion criteria

-

Treatment and study plan

hypothermia therapy

Other

newborn infants with hypoxic-ischaemic encephalopathy are cooled for 72 hours with a target temperature of 33-34°C (whole body cooling).

Primary outcomes

  1. neurodevelopmental outcome at 18-24 month of Age

    Time frame: 7 years

    The investigators will analyse if there is a correlation of placenta histology and neurodevelopmental outcome

Sponsors and collaborators

Lead sponsor

University Children's Hospital, Zurich

Other

Registry information

Important dates

Study start
2011
Primary completion
2017
Study completion
2017
First posted
Sep 15, 2017
Registry last updated
Sep 21, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.