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Blood Collection to Validated New Therapeutics Strategies Against Preeclampsia

New Therapeutic Strategy Against Preeclampsia: Angiogenic Switch to Physiological State by Extracorporeal Removal of sFlt-1

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03188900
Acronym
APHERESE
Enrollment
236
Registered
2017-06-16
Start date
2017-06-12
Completion date
2019-06-12
Last updated
2026-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Preeclampsia

Keywords

Preeclampsia, apheresis, sflt-1

Brief summary

The aim of the study is to setup a collection of maternal plasma and serum from patients with preeclampsia and normal pregnancy for in vitro validation of new therapeutics based on extra-corporal removal of sFlt-1

Detailed description

A collection of maternal plasma and serum from patients with preeclampsia (PE) and normal pregnancy (NP) : * Between 20WG and 23WG+6D : 20 patients with PE and 30 patients with NP * Between 24WG and 27WG+6D : 20 patients with PE and 30 patients with NP * Between 28WG and 31WG+6D : 20 patients with PE and 30 patients with NP * Between 32WG and 35WG+6D : 20 patients with PE and 30 patients with NP * Between 36WG and 40WG+6D : 20 patients with PE and 30 patients with NP

Interventions

BIOLOGICALA collection of maternal plasma and serum

A collection of maternal plasma and serum from patients with preeclampsia (PE) and normal pregnancy (NP)

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER
INSERM UMR-S 1139
CollaboratorUNKNOWN
URC-CIC Paris Descartes Necker Cochin
CollaboratorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Age from 18 to 50 years old * Singleton pregnancies between 20 and 41 weeks of gestation * Preeclampsia * Normal pregnancy

Exclusion criteria

* Age\<18 * Infectious disease: HIV, HBV or HCV * Multiple pregnancies * Opposition of the patient

Design outcomes

Primary

MeasureTime frameDescription
ratio sFlt-1/PlGFDay 0measurement of of sFlT-1 and PlGF

Secondary

MeasureTime frameDescription
Kinetics of these ratios sFlt-1/PlGF during pregnancyuntil 5 monthmeasurement of of sFlT-1 and PlGF at many times

Countries

France

Contacts

STUDY_DIRECTOREdouard Lecarpentier, MD, PhD

Centre Hospitalier intercommunal de Créteil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 28, 2026