effects of Progesterone by vaginal suppository to reduce preterm birth in women at risk
Phase 3
- Conditions
- Preterm delivery.Pregnancy, childbirth and the puerperium(O00-O99)
- Registration Number
- IRCT201108286808N2
- Lead Sponsor
- Birjand University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 56
Inclusion Criteria
cervical insufficiency, history of premature labor and uterine abnormalities.
Exclusion criteria :
fetal abnormalities, preeclampsia, and sensitivity to progesterone
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umber of days delay in delivery of prescribed suppositories. Timepoint: during labor. Method of measurement: Counting the days.
- Secondary Outcome Measures
Name Time Method