Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:16 AM
Ignite Modification Date:
2025-12-25 @ 2:16 AM
NCT ID:
NCT04170660
Eligibility Criteria:
Inclusion Criteria:
* Age ≥ 18 years old
* Pregnant patients term ≥ at 24 weeks of amenorrhoea (SA),
* Management in obstetrical emergencies and at the Centre Hopsitalier Intercommunal (CHI) de Créteil functional exploration center, with prescription of a vascular-renal check-up (BVR) ((proteinuria/creatinuria ratio, blood count, platelets, blood ionogram, creatinemia, transaminases (ASAT, ALAT), haptoglobulinemia, lactate dehydrogenase (LDH), TP).
* Presenting either one of the following isolated or associated clinical parameters:
* HyperTension
* urinary tape proteinuria
* functional signs of hypertension (headaches, phosphenes, accouphènes)
* live osteotendinous reflexes
* epigastric pains
* weight gain, lower limb edema, facial edema
* oliguria
* vomiting
* or one of the following isolated or associated ultrasound parameters:
* fetal hypotrophy, fetal growth deflection
* fetal Doppler abnormalities (umbilical Doppler, cerebral Doppler)
* ooligo-anamnios with intact membranes
* patient who has been informed and has given her oral non-opposition
Exclusion Criteria:
* Diagnosis of preeclampsia
* Refusal of the patient
* Patient whose symptomatology (clinical or paraclinical) leads to a decision to be hospitalized
* Age \< 18 years old
* Non-affiliation to the general social security system
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT04170660
Study Brief:
Protocol Section:
NCT04170660