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.

Marie Maroun-Aouad
mm01@aub.edu.lb

24299932
Completed

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


No
Collaborators
  • Sahar Siddik-Sayyed
  • Samar Taha-Bohsaly
  • Ghassan Kanazi
Coordinators
Fadia Shebbo
fs97@aub.edu.lb
Extension: 5411
Conditions and Keywords
physician interventions during spinal anesthesia for elective cesarean delivery
spinal anesthesia; caesarian delivery; Phenylephrine Infusion; hypotension
Study Design
Case Control
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.