Status:
COMPLETED
Effect of Intraoperative Lidocaine Infusion on Intraoperative Isoflurane Requirements
Lead Sponsor:
Assiut University
Conditions:
Anesthesia
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
Fifty patients were included in the study, divided into two equal groups (25 in each), underwent spinal fusion surgery.Control group: received normal saline. Lidocaine group: received lidocaine 2.0 m...
Detailed Description
This prospective, double-blinded, randomized study was carried out in Assiut University Hospitals, after approval by the local research ethics committee of Assiut Faculty of Medicine, Egypt. Informed ...
Eligibility Criteria
Inclusion
- Adult patients underwent spinal fusion surgery ASA I, II and III
Exclusion
- History of epilepsy hearing disorders known allergy to lidocaine BMI \> 35 significant cardiac diseases significant renal diseases liver dysfunction substance abuse chronic opioid use
Key Trial Info
Start Date :
October 2 2016
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 15 2017
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT03386565
Start Date
October 2 2016
End Date
December 15 2017
Last Update
December 29 2017
Active Locations (0)
Enter a location and click search to find clinical trials sorted by distance.
No Results Found
We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.