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Clinical Trial Summary

The primary aim of this study is to identify potential anthropometric features that predict the relationship between the Interscalene Block procedure and changes in blood pressure


Clinical Trial Description

This prospective, randomized study will be carried out after obtaining the necessary ethical approval and informed consent from the patients. 110 adult volunteer patients who will undergo ISB for shoulder surgery anesthesia will be included in this study. Evaluation of the patients before ISB and anthropometric measurements before and after Interscalene Block will be performed by an anesthesiologist who is not involved in the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06394960
Study type Observational
Source Konya City Hospital
Contact Mahmut S TUTAR
Phone +903322111576
Email masatu42@gmail.com
Status Recruiting
Phase
Start date May 2, 2024
Completion date August 5, 2024