Comparison of delaying in premature labour by indomethacin and Mg sulfate in pregnant women referred to maternity hospital
Not Applicable
- Conditions
- premature labour pain.Preterm labour without delivery
- Registration Number
- IRCT138811223329N1
- Lead Sponsor
- Kashan University of Medical Sciences and Health Services
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
gestational age 24-32 based on LMP and sonography during first trimester, single pregnancy, intact membrane, lack of GI or kidney disease, myasthenia gravis
Exclusion criteria: rupture membrane, vaginal bleeding, dilatation = 5 centimeter, placenta and fetal abnormalities, allergy to indomethacin, tocolytic therapy
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method terine contraction. Timepoint: every 15 minutes until 1 hour. Method of measurement: palpation of uterine contraction via abdomen.
- Secondary Outcome Measures
Name Time Method Vaginal bleeding. Timepoint: during 48 hours. Method of measurement: self reporting.;Rupture of membrane. Timepoint: during 48 hours. Method of measurement: self reporting.;Duration of delivery delaying. Timepoint: during 48 hours. Method of measurement: control of contraction.;Fetal heart rate. Timepoint: during 48 hours. Method of measurement: sonicade.