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Effect of supplementation in treatment of pregnancy complications

Phase 3
Conditions
Pre-eclampsia.
Sequelae of complication of pregnancy, childbirth and the puerperium
Registration Number
IRCT201102135444N3
Lead Sponsor
Vice chancellor for research, Kashan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
60
Inclusion Criteria

Primigravida pregnant women
Aged 18–40 years old
At risk for pre-eclampsia
Lived approximately 20 km or less from the clinic and hospital

Exclusion Criteria

Hypertension
Renal diseases
Gestational diabetes mellitus (GDM)
Abnormal foetal anomaly scan

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pre-eclampsia rate. Timepoint: After delivery. Method of measurement: Medical record.;Low birth weight (LBW) (<2500 g). Timepoint: After delivery. Method of measurement: Scale.;Newborn's birth size. Timepoint: After delivery. Method of measurement: Scale and tape.;Preterm delivery (<37 weeks). Timepoint: After delivery. Method of measurement: Medical record.
Secondary Outcome Measures
NameTimeMethod
Insulin. Timepoint: Baseline and End-of-trial. Method of measurement: Eliza.;Nitric oxide. Timepoint: Baseline and End-of-trial. Method of measurement: Spectrophotometry.;High-sensitivity C-reactive protein. Timepoint: Baseline and End-of-trial. Method of measurement: Eliza.;Total antioxidant capacity. Timepoint: Baseline and End-of-trial. Method of measurement: Spectrophotometry.;Fasting plasma glucose. Timepoint: Baseline and End-of-trial. Method of measurement: Enzymatic.;Triglyceride. Timepoint: Baseline and End-of-trial. Method of measurement: Enzymatic.;Cholesterol. Timepoint: Baseline and End-of-trial. Method of measurement: Enzymatic.;HDL-cholesterol. Timepoint: Baseline and End-of-trial. Method of measurement: Enzymatic.;Blood pressures. Timepoint: Baseline and End-of-trial. Method of measurement: Manometer.
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