Ketamine for Analgesia After Cesarean Section

Status Completed

Clinical Trial Summary

In this prospective randomized trial, investigators compared the analgesic effect of subanesthetic dose of ketamine versus placebo in parturients undergoing cesarean section under spinal anesthesia.

Clinical Trial Description

In this prospective randomized trial, investigators compared the analgesic effect of subanesthetic dose of ketamine versus placebo in parturients undergoing cesarean section under spinal anesthesia.

The patients were randomized in two groups:

- Group Ketamine: these patients recieved 0.25 mg/kg of Ketamin intravenously 5 minutes after the spinal anesthesia.

- Group Placebo: recieved 20 ml of normal saline solution intravenously 5 minutes after the spinal puncture.

The investigators recorded intra demographic, intraoperative and post operative data.

The main outcome was the analgesic score: the visual analog scale (VAS). dynamic VAS was also monitored at 24 hours post operatively. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04545801
Study type	Interventional
Source	Mongi Slim Hospital
Contact
Status	Completed
Phase	N/A
Start date	January 1, 2019
Completion date	April 30, 2019

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