Study of Microvesicles in Pre-eclampsia

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

A large number of studies on MVs from syncytiotrophoblasts support the hypothesis of their involvement in pre-eclampsia, via their multiple effects, among others as pro-coagulant, immuno-stimulatory and anti-angiogenic factors. The main objective is to compare the total concentration of the main populations of MVs in the maternal blood of a population of pre-eclamptic patients to those of a population of non-pre-eclamptic patients.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: t
View:

• Age ≥ 18 years

• Singleton pregnancy (or spontaneously reduced twin pregnancy before 14 SA)

• Gestational age at inclusion between 23 and 31+6 SA

• Collection of the patient's non-opposition

• Affiliated or beneficiary of a social security system

• Specifically for the non-pre-eclampsia group: non-pre-eclamptic patient hospitalized for isolated threat of preterm delivery, whatever the origin, and without clinical (absence of maternal hyperthermia defined by a maternal temperature \< 38.0°C) or biological markers of inflammation (CRP\<5)

• Specifically for the pre-eclampsia group : diagnosis of severe pre-eclampsia before 32 weeks' gestation

Locations
Other Locations
France
CHU Bordeaux
RECRUITING
Bordeaux
Contact Information
Primary
Loic Sentilhes, MD, PhD
loic.sentilhes@chu-bordeaux.fr
+335 57 82 23 36
Backup
Alain Brisson, PhD
a.brisson@cbmn.u-bordeaux.fr
Time Frame
Start Date: 2023-05-31
Estimated Completion Date: 2025-12
Participants
Target number of participants: 20
Treatments
Experimental: Pre-eclamptic women
The intervention consists of the collection of 2 additional tubes of 4.5mL of citrate blood. The sample will be collected as close as possible to the diagnosis of pre-eclampsia during a routine care assessment
Active_comparator: Non pre-eclamptic women
The intervention consists of the collection of 2 additional tubes of 4.5mL of citrate blood. sampling will be performed during routine care according to the matching.
Related Therapeutic Areas
Sponsors
Collaborators: University of Bordeaux
Leads: University Hospital, Bordeaux

This content was sourced from clinicaltrials.gov