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Evaluation of the effect of vaginal progesterone administration on ultrasonographic indicators and fetal and pregnancy outcomes of women at high risk of preeclampsia

Evaluation of the effect of vaginal progesterone administration on ultrasonographic indicators and fetal and pregnancy outcomes of women at high risk of preeclampsia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20151228025732N72
Enrollment
60
Registered
2022-09-05
Start date
2022-09-11
Completion date
Unknown
Last updated
2022-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High risk pregnancy. Supervision of high risk pregnancy

Interventions

Intervention 1: Intervention group: In this group
Treatment with oral aspirin tablets (Cardiosprin 80 grams, manufactured by Samisaz, Iran) on a daily basis from the 12th week of pregnancy to the 36th week
Together with vaginal progesterone suppositories (Cyclogest 400 mg, manufactured by Octoverco, Iran) daily from the 12th week of pregnancy to the 34th week. Intervention 2: Control group: In this grou
Treatment with oral aspirin tablets (Cardiopirin 80 grams, manufactured by Samisaz Company, Iran) is performed daily from the 12th week of pregnancy to the 36th week.

Sponsors

Semnan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSatinik Darzi

Semnan University of Medical Sciences

are20935@gmail.com+98 23 3345 1336

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026