O14.9
Conditions
Interventions
Group 1: 15 preeclamptic patients will be treated with H.E.L.P. apheresis or double filtration apheresis (case group)
Group 2: 15 pregnant women without preeclampsia (control group)
Group 3: cord bloo
Sponsors
Universitätsklinikum Freiburg, Institut für Klinische Chemie und Laboratoriumsmedizin
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Pregnant women with early preeclampsia ( 18 years
Exclusion criteria
Exclusion criteria: Pregnant women: every acute indication for immediate delivery; fetal blood cord: every medical reason against the blood withdrawal
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Prolongation of pregnancy | — |
Secondary
| Measure | Time frame |
|---|---|
| Pregnant women with apheresis (case group): proteinuria, blood pressure, clinical symptoms, sonographic criteria in doppler ultrasound of umbilical vessels, quantity of amniotic fluid, concentrations of lipoproteins seperated by density gradient ultracentrifugation, fibrinogen, sFlt-1 und PlGF, Lp-PLA2, blood cell count, haptoglobin, serum kreatinine, GOT, GPT, blood viscosity; in vitro: effect of biochemical parameters and diverse lipoprotein fractions on vasoactive receptors in cell cultures, analysis of parameters in the eluate of the apheresis filter; pregnant women (control group): concentrations of lipoproteins seperated by density gradient ultracentrifugation, fibrinogen, sFlt-1 und PlGF, Lp-PLA2, blood cell count, differential blood count, haptoglobin, serum kreatinine, GOT, GPT, blood viscosity; cord blood (case and control group): pH,total cholesterol, triglycerides, lipidelectrophoresis, lipid density gradient ultracentrifugation, Lp(a), Lp-PLA2, sFLT, PlGF; newborn (case group): weight, body height, pH of umbilical cord blood, APGAR, severe respiratory distress syndrome, duration of mechanical ventilation, intracranial hemorrhage (grade 1-4), necrotising enterocolitis, sepsis, duration of stay in intensive care unit, need of surfactant; newborn (control group): weight, body height, APGAR | — |
Countries
Germany
Contacts
Public ContactBrigitte König
Universitätsklinikum Freiburg, Institut für Klinische Chemie und Laboratoriumsmedizin
Outcome results
None listed