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Axillary Approach to Brachial Plexus Blockade Using Ketamine, Regional Versus Intravenous Administration

Anesthesia Clinical Trial

Official title:
Administration of Ketamine to Branchial Plexus Block Using Axillary Approach : Comparative Study

Clinical Trial Summary

The purpose of this study is to assess Ketamine as an adjuvant to Branchial Plexus Blockade.

Clinical Trial Description

After being informed about the study, patients giving written informed consent will undergo anaesthesia using the Ultrasound Guided Axillary Approach to Brachial Plexus Blockade, in order to undergo forearm surgery. The purpose of this study is to assess whether Ketamine as an adjuvant lengthens sensory and motor blockade and whether it has an effect on "rebound pain" when the anaesthetic effect fades. Therefore the study will compare intravenous, regional and no administration of Ketamine as an adjuvant to Branchial Plexus Blockade. Patients will be asked to fill in a Pain VAS (Visual Analog Scale) for 24 hours following the intervention, in order to assess effectiveness of each anaesthetic method. Side effects, onset time, motor blockade score and rescue dose are also recorded. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05297422
Study type Interventional
Source National and Kapodistrian University of Athens
Contact Demetra Solomou
Phone +306987707097
Email Demetra_Sol@hotmail.com
Status Recruiting
Phase N/A
Start date January 20, 2022
Completion date June 2023
View Details
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