Clinical Research Details

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

Marie Maroun-Aouad
mm01@aub.edu.lb

19641050
Completed

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


No
Collaborators
  • Sahar Siddik Sayyed
  • Viviane Nasr
  • Samar Taha-Bohsaly
  • Anis Baraka
Coordinators
Fadia Shebbo
fs97@aub.edu.lb
Extension: 5411
Conditions and Keywords
Elective Cesarean Delivery
Cesarean Delivery; 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. On arrival to the operating room, an 18-gauge IV cannula was placed on the left arm/hand of the patient, and lactated Ringer’s solution was connected to keep the IV line patent