Effect of painless vaginal delivery versus normal vaginal delivery on maternal and neonatal outcomes in pregnant wome
Phase 2
- Conditions
- Vaginal delivery.Other obstructed labour
- Registration Number
- IRCT201508259014N77
- Lead Sponsor
- Vice-chancellor for Research the Technology, Hamadan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 168
Inclusion Criteria
(a) gestational age of 37 weeks or over; (b) being eligible for vaginal delivery.
Exclusion criteria: (a) having diabetes, cardiovascular diseases, or intracranial diseases; (b) having gestational diabetes, preeclampsia, or macrosomia; (c) coagulation disorders; (d) dermal infection on the location of epidural anesthesia; (e) non-treated bacteremia.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Measuring the duration of the first and second stages of vaginal delivery. Timepoint: after intervention. Method of measurement: using Friedman curve.;Measuring episiotomy pain. Timepoint: 6 and 12 hours after vaginal delivery. Method of measurement: using visual analog scale (VAS).;) assessing Apgar score. Timepoint: at the first and fifth minutes after birth. Method of measurement: through physical examination.
- Secondary Outcome Measures
Name Time Method Assessing hyperthermia. Timepoint: at 4, 8, and 12 hours after vaginal delivery. Method of measurement: using oral thermometer.;Assessing headache. Timepoint: 12 hours after vaginal delivery. Method of measurement: using visual analog scale (VAS).