Ketamine molecule:

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Ketamine Clinical Trials


Analgesia Effects of Intravenous Ketamine After Spinal Anesthesia for Non-elective Cesarean Section


To see complete record on clinicaltrials.gov, please visit this link

Id: NCT03450499

Organisation Name: B.P. Koirala Institute of Health Sciences

Overal Status: Completed

Start Date: April 1, 2018

Last Update: August 20, 2019

Lead Sponsor: B.P. Koirala Institute of Health Sciences

Brief 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.

Conditions:
  • Non Elective Cesarean Section and Ketamine Analgesia


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