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Preload versus coload of ringer lactate to prevent hypotension during elective cesarean section under spinal anesthesia

Phase 3
Recruiting
Conditions
Hypotension during cesarean section.
Hypotension
Registration Number
IRCT20110313006044N5
Lead Sponsor
Vice-Chancellery for Research Hormozgan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

Age 18-45 years
Singleton term pregnancy
Elective cesarean section
Spinal anesthesia
American Society of Anesthesiologists (ASA) class I or II

Exclusion Criteria

Twin or multiple pregnancy
ASA class above II
Hypertension or cardiovascular diseases
Contraindications of spinal anesthesia
Hypersensitivity to bupivacaine
Renal disorders
Severe hemorrhage during surgery requiring blood transfusion
Uterine atony requiring hysterectomy
Block failure or incomplete block demanding extra anesthetics

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Maternal blood pressure. Timepoint: Baseline, immediately after spinal anesthesia, then at 2, 4, 6, 8, 10, 15, 20, 25, 30, 40, 50, and 60 min after spinal anesthesia and in the recovery unit. Method of measurement: Monitoring device.
Secondary Outcome Measures
NameTimeMethod
Maternal mean arterial pressure. Timepoint: Baseline, immediately after spinal anesthesia, then at 2, 4, 6, 8, 10, 15, 20, 25, 30, 40, 50, and 60 min after spinal anesthesia and in the recovery unit. Method of measurement: Monitoring device.;Maternal heart rate. Timepoint: Baseline, immediately after spinal anesthesia, then at 2, 4, 6, 8, 10, 15, 20, 25, 30, 40, 50, and 60 min after spinal anesthesia and in the recovery unit. Method of measurement: Monitoring device.;Maternal oxygen saturation. Timepoint: Baseline, immediately after spinal anesthesia, then at 2, 4, 6, 8, 10, 15, 20, 25, 30, 40, 50, and 60 min after spinal anesthesia and in the recovery unit. Method of measurement: Monitoring device.;Neonatal Apgar score. Timepoint: 1 and 5 min after delivery. Method of measurement: Clinical assessment.
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