Effect of vaginal progesterone on prevention of preterm delivery and neonatal side effects in women at risk for preterm birth
Phase 2
Recruiting
- Conditions
- Preterm Labor Birth.Preterm labour with preterm delivery
- Registration Number
- IRCT201012273386N2
- Lead Sponsor
- Semnan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 100
Inclusion Criteria
Inclusion: history of preterm labor birth (having at least one delivery before 37 wks of gestational age), incompetent cervix and having cerclage, uterine anomalies (septate uterus. unicornuate or bicornuate). exclusion: clinical evidence of chorioamnionitis, contraindication to use of progesterone (allergy to progesterone products, Diabetes, hypertension, hyperthyroidism, heart disease, polyhydramniose. IUGR, multiple pregnancy.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Preterm Labor Birth. Timepoint: From 16 week to 34 week. Method of measurement: Delivery.
- Secondary Outcome Measures
Name Time Method ecrotising Entrocolitis. Timepoint: After Birth. Method of measurement: NICU records.;Intra Cranial Haemorrhage. Timepoint: After Birth. Method of measurement: NICU records.;Weight less than 2500 g. Timepoint: After Birth. Method of measurement: scale.