The effectiveness of entonox during labor
- Conditions
- single spontaneous delivery.Other single spontaneous delivery
- Registration Number
- IRCT2015102713159N6
- Lead Sponsor
- Vice Chancellor for Research, Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 400
Being primigravida; aged between 18 and 40 years; term pregnancy (37-42 weeks); single gestation pregnancy; normal embryo; not having any midwifery care and medical problems (e.g., cardiovascular problems and other internal diseases); not using other analgesics and anesthetics; not having any medical restrictions on entonox gas inhalation (due to respiratory diseases, pneumothorax, or past history of head trauma); and normal fetal heart rate patterns.
Exclusion criteria: Not being primigravia; embryo anomalies; having any complications during labor and delivery; need for cesarean section; use of other anesthetics and analgesics; having medical restrictions on entonox gas inhalation (respiratory diseases, pneumothorax, or previous history of head trauma); and abnormal fetal heart rate pattern
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Rang of pain intensity during labor. Timepoint: Each 15 minets. Method of measurement: Numeric scale rating / Number.
- Secondary Outcome Measures
Name Time Method Maternal heart rate. Timepoint: In minutes. Method of measurement: Compact monitoring device / The number in minutes.