The Effect of Entonox on Labor Pain and Outcome of Delivery among Primi-Parrous Women Reffered to Atieh Hospital in Hamadan, 2014
Phase 2
- Conditions
- abor.Single spontaneous delivery
- Registration Number
- IRCT2014060210426N2
- Lead Sponsor
- Hamadan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 70
Inclusion Criteria
full term pregnant women; single pregnancy; primiparous; aged between 18-35 years old; vertex presentation; normal pelvic and no stimulation before study.
Exclusion criteria: having a systematic chronic diseases e.g. hypertension, diabetes, asthma, vaginal bleeding; twin pregnancy; multiparous and stimulation before study.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Relief of Labor pain. Timepoint: Initial, after one hour, after two hours, after three hours, after four hours. Method of measurement: Visual Analog Scale (VAS).
- Secondary Outcome Measures
Name Time Method Duration of labor. Timepoint: Initial, after one hour, after two hours, after three hours, after four hours. Method of measurement: Duration of labor per hour.