Comparison of ketorolac-induced analgesia with ketamine in lumbar fusion surgery patients using PCA pain pump

Phase 3

Recruiting

• Conditions: umbar fusion.; Fusion of spine, lumbar region; M43.26

• Registration Number: IRCT20160403027191N5
• Lead Sponsor: Mazandaran University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 November 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

The patient's willingness to participate in the study and obtain informed consent
Performing lumbar fusion surgery during the research
Being 20 to 75 years old

Exclusion Criteria

History of previous spine surgery
Known hypersensitivity to ketamine or ketorolac
Occurrence of any unusual complications during surgery
Substance abuse and psychoactive drugs

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Intensity of pain. Timepoint: at 2, 4, 6, 12, 18, 24 hours after surgery. Method of measurement: check list.

Secondary Outcome Measures

Name	Time	Method
Time of return from Ileus. Timepoint: At times 2, 4, 6, 12, 18, 24 hours after surgery. Method of measurement: check list.;Nausea and vomiting. Timepoint: At times 2, 4, 6, 12, 18, 24 hours after surgery. Method of measurement: check list.