Checking the effect of oral Dydrogesterone (Duphaston) on preventing preterm labor
Not Applicable
Recruiting
- Conditions
- Preterm labor.Preterm labor
- Registration Number
- IRCT20190107042266N1
- 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
From the age of 18 to 45
Gestational age of 24 to 34 weeks (calculation based on first trimester sonography)
Not having PLP 48 hours after treatment
Single pregnancy
Not of smoking
Exclusion Criteria
Placenta Previa
Premature rupture of membranes
Chorioamnionitis
Severe preeclampsia
The use of progesterone before the study
Contraindication of progesterone
Contraindication of Tocolytic
Dilatation more than 4 centimeters
Fetal anomalies
Dissatisfaction of the patient to continue participating in the study
Pregnancy scar
Cervical cerclage
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Preterm labor before the 37th week of pregnancy. Timepoint: From the beginning of the intervention (from the beginning of preterm labor up to the gestational age of 24 to 34 weeks) until the occurrence of the preterm labor (gestational age of 36 weeks and 6 days). Method of measurement: Visiting the patient every other two weeks for the relapse of preterm labor pain, regular use of drugs, drug based side effects like nausea, dizziness and exhaustion.
- Secondary Outcome Measures
Name Time Method