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Efficacy of Voluven® for the Prevention of Hypotension During Spinal Anesthesia for Cesarean Section - NCT00694343-Lille - 004(Clinical Trial 225546)



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City:  Lille
Country:  
France
Conditions: Hypotension
Purpose: The aim of the study is to evaluate the efficacy of Voluven® in the prevention of maternal hypotension in women undergoing spinal anesthesia for cesarean section
Study summary: Intravenous fluid administration prior to spinal anesthesia for cesarean section is an established part of anesthetic practice for the prevention of maternal hypotension. Systematic reviews of clinical data suggest the usefulness of administering colloids to decrease the incidence of hypotension This study will compare the clinical efficacy and safety of HES 130/0.4 (6%) in normal saline vs. Ringer's lactate solution in prevention of hypotension during spinal anesthesia for elective cesarean section.
Criteria: Inclusion Criteria: - elective cesarean section applying spinal anesthesia - ≥ week 37 of gestation - Singleton pregnancy Exclusion Criteria: - Suspicion of any hypertensive disease - Parturient in labor
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Data Source: ClinicalTrials.gov
Date Processed: February 1, 2010
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