mild preeclampsia. Mild to moderate pre-eclampsia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Pregnant women with mild preeclampsia singleton pregnancy with live fetus Gestational age more than 24 weeks Women with first pregnancy (Noliparus) Suitable maternal and fetal conditions for expectant management
Exclusion criteria
Exclusion criteria: Women with cardiovascular disease Women with renal and hepatic dysfunction Extreme and chronic hypertension Gestational diabetes mellitus and chronic History of probiotic susceptibility Use of antibiotics over the past two weeks
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mean systolic and diastolic blood pressure. Timepoint: Blood pressure will be measured before, during and after the study. Method of measurement: Measurement of blood pressure by ISOMED mercuric barometric device.;Mean duration of pregnancy from diagnosis to delivery. Timepoint: A the time of delivery. Method of measurement: Duration of pregnancy by calculating LMP or first trimester ultrasound.;Mean of newborn weight at birth. Timepoint: A the time of delivery. Method of measurement: Measurement of birth weight by SECA scales. | — |
Secondary
| Measure | Time frame |
|---|---|
| Detection of severe preeclampsia. Timepoint: During the study. Method of measurement: Criteria for the diagnosis of severe preeclampsia in the questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tabriz University of Medical Sciences