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The effects of crystalloid or colloid on maternal blood pressure after spinal anesthesia in cesarean section.

Phase 2
Conditions
Cesarean Section.
Complications of anaesthesia during labour and delivery
Registration Number
IRCT201307215381N6
Lead Sponsor
Vice-chancellor of Research Babol University Of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
105
Inclusion Criteria

18 to 35 years pregnant women candided for cesarean secton with ASA class I,II; parturients more than 37-week gestation.
Exclusion criteria: Hypertension BP>140/90; DM;weight >100 kg; multiple gestation; Cardiovascular and cerbrovascular disease; Significant fetal abnormalities; contraindication of spinal anesthesia; mothers who are at the start of active phase of labor

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Blood pressure. Timepoint: Baseline BP before Spinal anesthesia and every 3 minutes control until the end of surgery. Method of measurement: Non invasive BP Cuff.;PH of umbilical artery. Timepoint: Immediatly after birth. Method of measurement: ABG.
Secondary Outcome Measures
NameTimeMethod
Base excess. Timepoint: Base excess. Method of measurement: ABG.;Lactate of umbilical artery. Timepoint: Immediatly after birth. Method of measurement: ABG.;Infant Apgar. Timepoint: 1 and 5 minutes after birth. Method of measurement: Apgar Score.;Heart rate. Timepoint: Before spinal anesthesia until the end of surgery every3 minutes. Method of measurement: pulse counting.
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