delivery. Single spontaneous delivery
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: singleton pregnancy estimated fetal weight 2500-4000 cephalic presentation normal FHR no use of analgesic and opium from 48h before entrance into trial spontaneous labor pain normal back skin no history of cesarean section no contraindication of NVD no history of cardiorespiratory disease no history of psychology disorders no history of hearing disorders active phase of labor
Exclusion criteria
Exclusion criteria: patient unwillingness to continue cooperation indications for augmentation during labor indications for emergent C/S
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain score during labor. Timepoint: Before intervention, every 1 hour during active phase of labor till delivery. Method of measurement: visual analogue scale for measurement of pain with questionnaire.;Pain score in postpartum. Timepoint: Every 2 hours till 4 hours after delivery and every 6 hours till 24 hours after delivery. Method of measurement: visual analogue scale for measurement of pain with questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| Satisfaction. Timepoint: 24 hours after delivery. Method of measurement: questionnaire.;Duration of active phase. Timepoint: From entrance to active phase till full dilatation of cervix. Method of measurement: hour.;Duration of stage 2 labor. Timepoint: From full cervical dilatation till delivery. Method of measurement: minuets.;Neonatal APGAR. Timepoint: 1 and 5 minutes after birth. Method of measurement: APGAR scoring system.;Analgesic usage in postpartum. Timepoint: 24 hours after delivery. Method of measurement: Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Shahid Beheshti University of Medical Sciences