Comparison of two drugs for Preterm Labor
- Conditions
- preterm labor.Preterm labour and delivery
- Registration Number
- IRCT201012155401N1
- Lead Sponsor
- Hamadan university of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 100
all high risk women for pre-term labour including: recurrent abortion, pre tem labour history, cervical rippening, etc. Exclusion criteria: Epileptic and asthmatic subjects; those with uncontrolled diabetes; those who were sensitive to progesterone; those who have received progesterone four weeks before the study; mental illness; chronic HTN; active liver disorder; HIV infection or 35> CD4 count and anti-viral drug recipients; placenta previa; history of genital and breast cancer; history of thromboembolic disease and mullerian anomaly; ultrasound diagnosed major anomaly; recognized fetal chromosomal abnormalities; Multiple cerclage and preterm labor and PROM and clinical chorioamnionitis; vaginal bleeding and history of spontaneous preterm labor without delivery (including preterm labor).
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Preterm labor. Timepoint: monthly. Method of measurement: questionnaire and physical exam.
- Secondary Outcome Measures
Name Time Method Delivery type. Timepoint: monthly. Method of measurement: questionnaire.