PlGF as a diagnostic test for pre-eclampsia

Not Applicable

Completed

• Conditions: Specialty: Reproductive health and childbirth, Primary sub-specialty: Reproductive and sexual medicine; UKCRC code/ Disease: Reproduction/ Other disorders originating in the perinatal period; Pregnancy and Childbirth; Pre-eclampsia

• Registration Number: ISRCTN16842031
• Lead Sponsor: Guy's and St Thomas' NHS Foundation Trust (UK)

Brief Summary

2019 results in: https://www.ncbi.nlm.nih.gov/pubmed/30948284

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-05-19
• Study Completion: 2018-03-31
• Last Update Posted: 5 May 2019

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 504

Inclusion Criteria

1. Women between 20+0 and 36+6 weeks’ of gestation
2. Suspected pre-eclampsia
3. Viable fetus
4. Singleton
5. Aged 18 years or over
6. Able to give written informed consent

Exclusion Criteria

Confirmed diagnosis of preterm pre-eclampsia at the point of enrolment

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<br> Time from first presentation with hypertension to antenatal services to having a confirmed, documented diagnosis of pre-eclampsia (as defined by ISSHP 2014 statement). The time points of evaluation are first presentation with suspected disease to confirmed diagnosis of pre-eclampsia. This is a participant level outcome.<br>