Effect of different methods of remifentanil administration in labor pai
Not Applicable
- Conditions
- Single spontaneous delivery.cases with minimal or no assistance, with or without episiotomy
- Registration Number
- IRCT2012100811020N2
- Lead Sponsor
- Zahedan University of Medical Sciences, Deputy of Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 82
Inclusion Criteria
primigravid healthy parturient with 37-42 weeks of pregnancy; in active stage of labor (uterine contraction 3 per 10 minutes, lasting for 30 to 40 seconds and cervical dilation >=3 cm); with vertex presentation. Exclusion criteria: parturient with positive history of preeclampsia; using psychiatric drugs; using opioid and alcohol; antenatal hemorrhage; fetal distress; BMI>30 or <20; multi tone and requesting for epidural analgesia.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of uterine contractions pain. Timepoint: Every 15 minutes from the onset of active phase of labor to delivery. Method of measurement: verbal numeric rating scale (VNRS).;First stage of labour duration. Timepoint: every 15 minutes in first stage of labour from 4 cm dilation up to 10 cm, and in second stage from 10 cm dilation up to delivery. Method of measurement: Time by minutes.
- Secondary Outcome Measures
Name Time Method Grading of sedation. Timepoint: every 15 minutes. Method of measurement: Modified Observer's Assessment of Alertness.