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Clinical Trials/IRCT20120910010800N10
IRCT20120910010800N10
Recruiting
Phase 3

A randomized study to compare the sensory levels of spinal anesthesia for elective cesarean section using crystalloid versus Voluven solution

Shahid Beheshti University of Medical Sciences0 sites120 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Hypotension due to drugs.
Sponsor
Shahid Beheshti University of Medical Sciences
Enrollment
120
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • singleton pregnancy
  • Elective cesarean section
  • Gestational age more than 36 weeks
  • Height more than 150 and less than 175 cm
  • Body mass index less than 35 kg/m2
  • Consent to study

Exclusion Criteria

  • Sensitivity to local anesthetics

Outcomes

Primary Outcomes

Not specified

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