Status:
COMPLETED
Cardiac Index Changes With Ephedrine, Phenylephrine, Ondansetron and Norepinephrine During Spinal Anesthesia
Lead Sponsor:
University Tunis El Manar
Conditions:
Cardiac Output, Low
Eligibility:
FEMALE
18-45 years
Phase:
PHASE4
Brief Summary
The purpose of the study is to evaluate the cardiac output changes after an intravenous bolus of ephedrine, phenylephrine, ondansetron or norepinephrine during a spinal anesthetic for a cesarean deliv...
Detailed Description
This study will be a prospective, randomized, double-blind controlled trial. After written and informed consent are obtained, the study participants are randomly assigned using a computer generated ta...
Eligibility Criteria
Inclusion
- ASA I / II
- Caesarean section, non-twinned
Exclusion
- heart disease
- HTA
- non-gestational diabetes
- pre-eclampsia
- sepsis
- BMI greater than 40
- contraindication to spinal anesthesia: patient refusal, medicinal allergy, long QT syndrome.
Key Trial Info
Start Date :
February 23 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 30 2018
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT03421860
Start Date
February 23 2017
End Date
March 30 2018
Last Update
August 29 2018
Active Locations (1)
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1
Tunis maternity and neonatology center, minisetry of public health
Tunis, Tunisia, 1007