Investigating the effect of Entonox on normal vaginal delivery labor and maternal hemodynamic changes and fetal apgar
Not Applicable
- Conditions
- labor.Single spontaneous delivery
- Registration Number
- IRCT201105176480N2
- Lead Sponsor
- Vice chancellory for research, Shahrekord university of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 60
Inclusion Criteria
primiparous women; pregnancy age of 38-42; non twin pregnancy with the cephalic view; being in the early active phase of delivery; having normal fetal heart pattern; weight between 60-80 Kgr. Exclusion criteria: having cardio and other internal disease.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method abor. Timepoint: one hour. Method of measurement: NSR digital proportional measurement.;Maternal respiration rate. Timepoint: one hour. Method of measurement: numeration.;Maternal blood pressure. Timepoint: one hour. Method of measurement: mercurial manometer.;Maternal heart rate. Timepoint: one hour. Method of measurement: using a device.
- Secondary Outcome Measures
Name Time Method Baby apgar. Timepoint: one and five minutes after the birth. Method of measurement: related questionnare.;Nausea and vomiting. Timepoint: during the delivery. Method of measurement: observation.