Clinical Research Details

Descriptive Information
A randomized controlled trial of variable rate phenylephrine infusion with rescue phenylephrine boluses versus rescue boluses alone on physician interventions during spinal anesthesia for elective cesarean delivery

Sahar Sayyid
ss01@aub.edu.lb

24299932
Completed

Clinical Research - Clinical Trials (phase 0, 1,2 3 & 4)  


No
Collaborators
  • Marie Aoaud Maroun
  • Samar Taha
  • Ghassan Kanazi
Conditions and Keywords
spinal anesthesia for elective cesarean delivery
phenylephrine infusion;spinal anesthesia
Study Design
Eligibility and IRB
Female
Min:
Max:
Yes
No







nonlaboring parturients >37 weeks’ gestation, ASA physical status I or II scheduled for elective cesarean delivery

allergy or hypersensitivity to phenylephrine, hypertension, multiple gestation, known fetal abnormalities, diabetes mellitus, polyhydramnios, body weight less than 50 and more than 100 kg, height less than 150 and more than 180 cm, major systemic disease, anemia (hemoglobin concentration <10 g/dL), or clotting diathesis.