CompletedNot Applicable

Prediction of Preeclampsia (PE) at 11-13 Week

China, Hong Kong, India10,935 participantsStarted 2016-12

Plain-language summary

This is an international multicentre prospective cohort study to validate the Bayes theorem based algorithms for the screening of pre-eclampsia (PE) in the first-trimester of pregnancy.

Who can participate

Age range18 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Aged ≥ 18 years * Singleton pregnancy * Live fetus * Provide Informed and written consent in the official language of the country Exclusion Criteria: * Unable to provide written Informed consent learning difficulties or serious mental illness or an inability to understand spoken and written the official language of the country. * Multiple Pregnancy * Non-viable fetus (missed spontaneous abortion or stillbirth)

What they're measuring

The false positive and true positive frequencies for screening for PE using the Bayes theorem based methods

Timeframe: At delivery

Trial details

NCT IDNCT03554681

SponsorChiu Yee Liona Poon

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2018-12

View on ClinicalTrials.gov More Pre-Eclampsia trials