Progesterone effect on threatened abortio
Phase 2
- Conditions
- abortion.Fetus and newborn affected by other maternal complications of pregnancy Spontaneous abortion, fetus
- Registration Number
- IRCT201012035294N1
- Lead Sponsor
- Vice chancellor for research,Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
pregnant women less than 20 weeks of gestation with sign and symptoms of threatened abortion like bleeding, abdominal pain and induction of cervical secretion where included in this study; Exclusion criteria: Lack of satisfaction, hypertension and avoidance of participating in the study were considered as exclusion criteria.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of abortion. Timepoint: at the end of study. Method of measurement: due to definition, fetal weight less than 500 grams and delivery before 20 weeks.
- Secondary Outcome Measures
Name Time Method Study the inflammatory cytokines of cervix. Timepoint: before and after treatment. Method of measurement: special kits & Eliza.