Analgesia Effects of Intravenous Ketamine After Spinal Anesthesia for Non-elective Cesarean Section
Status:
Completed
Trial end date:
2019-03-07
Target enrollment:
Participant gender:
Summary
This randomized double blind study will be conducted in pregnant woman planned for non
elective cesarean section under spinal anesthesia. Ketamine group will receive intravenous
0.25 mg/kg and placebo group will receive same amount of normal saline after spinal
anesthesia prior to skin incision. Postoperative outcomes measures are total opioid
consumption and pain scores for 24 hrs.