Determination of the effect of Entonox gas and B massage on the severity of labor pai
Not Applicable
- Registration Number
- IRCT20180128038535N2
- Lead Sponsor
- Saveh University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 69
Inclusion Criteria
Pregnant women aged between 18-35 years old
Women with first, second, third and fourth pregnancies
Gestational age between 37 to 41 weeks
Singletone pregnancy
Head of presentation(cephalic)
Women in dilatation 4-5 centimeter or more
Exclusion Criteria
High-risk pregnant women (presence of previous scars on the uterus and abdomen, diabetic women, preeclampsia and eclampsia, Polyhydramnious, Oligohydramnious, fetal death and etc.)
There are skin or lumbar problems in the lower back region in the massage group
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of pain in the active phase of the first stage and second stage of labor. Timepoint: Immediately before the intervention, 45, 90, 135, 180 and 225 minutes after intervention. Method of measurement: Visual analogue Scale of McGill Pain.;Type of delivery. Timepoint: After intervention. Method of measurement: Observation.
- Secondary Outcome Measures
Name Time Method Postpartum hemorrhage. Timepoint: After intervention in the third stage of labor. Method of measurement: Observation and estimation of bleeding based on the need for hemoglobin to be checked in the first 6 hours after delivery, blood transfusion, need for uterine massage or prescribe misoprostol.;Apgar score of the infant in the first and fifth minutes of birth. Timepoint: After intervention and delivery. Method of measurement: Neonate Apgar Scale.;The need for newborn resuscitation. Timepoint: After intervention and delivery. Method of measurement: Neonatal resuscitation according to national protocol.