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The effect of Dydrogesterone and Cyclogest on threatend abortio

Phase 3
Conditions
Threatened abortion.
Threatened abortion
Registration Number
IRCT20120104008611N8
Lead Sponsor
Qazvin University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
160
Inclusion Criteria

Gestational age 6 to 13 weeks
Observation of fetal heart rate
Vaginal bleeding
Uterine anomalies
Fetal anomalies

Exclusion Criteria

Patient unwillingness
Breast carcinoma
Lack of fetal heart rate
Severe liver problems
Genital carcinoma
Thromboembolic disorders
Epilepsy
Diabetes
Hypertension

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Threatened abortion. Timepoint: Before intervention and 2 weeks after the completion of the intervention. Method of measurement: Weekly visit.
Secondary Outcome Measures
NameTimeMethod
Preeclampsia. Timepoint: Up to 28 weeks monthly and until 36 weeks every two weeks and thereafter weekly until delivery. Method of measurement: Mercury Barometer.;Gestational Diabetes. Timepoint: Up to 28 weeks monthly and until 36 weeks every two weeks and then weekly until delivery. Method of measurement: Glucose tolerance test.;Preterm labor. Timepoint: Up to 28 weeks monthly and until 36 weeks every two weeks and then weekly until delivery. Method of measurement: Tocometry of uterus and delivery before 37 weeks of pregnancy.;Low birth weight. Timepoint: Weight immediately after birth. Method of measurement: Pediatric scales.;Abortion under 20 weeks of pregnancy. Timepoint: Every week from the start of the intervention up to 20 weeks of pregnancy. Method of measurement: Questionnaire.
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