The effect of probiotic supplementation on pregnancy outcomes in mothers with mild preeclampsia

Phase 3

Recruiting

• Conditions: mild preeclampsia.; Mild to moderate pre-eclampsia; O14.0

• Registration Number: IRCT20110606006709N20
• Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 August 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 128

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

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

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
Detection of severe preeclampsia. Timepoint: During the study. Method of measurement: Criteria for the diagnosis of severe preeclampsia in the questionnaire.