Clinical Research Details

Descriptive Information
A randomized trial comparing colloid preload to coload during spinal anesthesia for elective cesarean delivery

Sahar Sayyid
ss01@aub.edu.lb

19641050
Completed

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


No
Collaborators
  • Vivianne Nasr
  • Samar Taha
  • Anis Baraka
  • Marie Aouad Maroun
Coordinators
Fadia Shebbo
fs97@aub.edu.lb
Extension: 5411
Conditions and Keywords
elective cesarean delivery
cesarean delivery;colloid preload;coload;spinal anesthesia
Study Design
Eligibility and IRB
Female
Min:
Max:
Yes
No







nonlaboring parturients more than 37-week gestation, ASA PS I or II scheduled for elective cesarean delivery

pregnancy-induced hypertension, chronic hypertension, multiple gestation, known fetal compromise, diabetes mellitus, polyhydramnios, weight >100 kg, major systemic disease, anemia (hemoglobin concentration <10 g/dL), or clotting diathesis