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Clinical Trials/NCT00199784
NCT00199784
Completed
Phase 4

Hemodynamic Measurements During Cesarean Section With Spinal Anesthesia

Oslo University Hospital1 site in 1 country80 target enrollmentJune 2005
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ConditionsHealthy
DrugsPhenylephrine

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Healthy
Sponsor
Oslo University Hospital
Enrollment
80
Locations
1
Primary Endpoint
Differences in cardiac output
Status
Completed
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of this study is to determine the effect of low dose versus standard dose spinal anesthesia with and without intravenous phenylephrine-infusion on blood pressure, cardiac output and systemic vascular resistance.

Detailed Description

Hypotension during cesarean section with spinal anesthesia is common. We compare low dose versus standard dose spinal anesthesia with and without intravenous phenylephrine-infusion.

Registry
clinicaltrials.gov
Start Date
June 2005
End Date
April 2007
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
Oslo University Hospital

Eligibility Criteria

Inclusion Criteria

  • •Healthy pregnant women for elective cesarean section
  • •Exclusion Criteria
  • •Shorter than 160 or taller than 180 cm
  • •Pre-pregnant body mass index (BMI) over 32

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Differences in cardiac output

Blood pressure

Systemic vascular resistance

Secondary Outcomes

  • Nausea
  • Fatigue
  • Cardiovascular instability due to overdosing spinal anesthesia for cesarean section (CS)

Study Sites (1)

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