Evaluation of the effect of vaginal progesterone administration on ultrasonographic indicators and fetal and pregnancy outcomes of women at high risk of preeclampsia
Not Applicable
Recruiting
- Conditions
- High risk pregnancy.Supervision of high risk pregnancy
- Registration Number
- IRCT20151228025732N72
- Lead Sponsor
- Semnan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
Age 18 and above
Body mass index above 30
The interval between pregnancies is more than 10 years
Multiple pregnancy
Pre-gestational diabetes
Live singleton fetus
Exclusion Criteria
Heart, liver, thyroid diseases, history of asthma
Aspirin sensitivity
Threatened abortion such as vaginal bleeding
Eclampsia and pre-eclampsia at the time of study
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Vascular Resistance Index (RI). Timepoint: Before the intervention and 6 weeks after the intervention. Method of measurement: Color Doppler ultrasound.;Pulsatile index (PI). Timepoint: Before the intervention and 6 weeks after the intervention. Method of measurement: Color Doppler ultrasound.
- Secondary Outcome Measures
Name Time Method