Comparing effect of the spinal anesthesia induced hypotension treatments on neonatal factors
Not Applicable
- Conditions
- Other complications of spinal and epidural anaesthesia during labour and delivery.Other complications of spinal and epidural anaesthesia during labour and delivery
- Registration Number
- IRCT2016062028545N1
- Lead Sponsor
- Vice Chancellor for Research of Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
interest to participate in study; obesity (BMI30 kg/m2); no underlying diseases except obesity; Class II category in ASA grading system; age between 18-40; term pregnancy; singleton pregnancy; candidate for elective cesarean section; candidate for epidural anesthesia.
Exclusion criteria: emergency cesarean section; diabetic mother; no consent to participate in study; gestational hypertension; epidural anesthesia contraindications; twin pregnancy; need to change epidural anesthesia to general anesthesia; intraoperative bleeding more than 1000 milliliter; neonate birth body weight less than 2500 grams.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method mbilical artery blood pH. Timepoint: Right after neonate birth. Method of measurement: Arterial blood gas test.;Umbilical artery blood pO2. Timepoint: Right after neonate birth. Method of measurement: Arterial blood gas test.;Umbilical artery blood pCO2. Timepoint: Right after neonate birth. Method of measurement: Arterial blood gas test.
- Secondary Outcome Measures
Name Time Method APGAR. Timepoint: APGAR in the first minute after delivery. Method of measurement: APGAR scoring system.;APGAR. Timepoint: APGAR in the fifth minute after delivery. Method of measurement: APGAR scoring system.