Clinical trial comparison of labor phases in painless delivery with epidural analgesia ?and Entonox
Not Applicable
- Conditions
- Delivery.Spontaneous vertex delivery
- Registration Number
- IRCT2016051820258N9
- Lead Sponsor
- Vice Chancellor For Research of Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 90
Inclusion Criteria
primigravida women; ?singleton pregnancies; term pregnancy of 37 to 42 weeks; no medical ?diseases; cervical dilation 3 - 4 centimeterv
Exclusion criteria: multiparous; multiple pregnancy; Preterm labor; Postterm labor
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Fetal heart rate. Timepoint: every 15 minute. Method of measurement: count.;Cervix dilatation. Timepoint: every 2 hours. Method of measurement: centimeter.;Apgar. Timepoint: after operation. Method of measurement: Apgar scale.;Complications after delivery. Timepoint: after operation. Method of measurement: question.
- Secondary Outcome Measures
Name Time Method