The Impact of a Beach Chair Position During Shoulder Arthroscopy on Regional Cerebral Oxygen Saturation : Comparison of Interscalene Block and General Anesthesia

Osijek University Hospital60 enrolled

Overview

The aim of this study is to investigate the relationship between the patient positioning in the beach chair position with consequential arterial pressure changes and their influence on regional cerebral oxygen saturation under two anesthesia techniques, general anesthesia in one group of patients and interscalene block in the second group of patients.

The participants of the study are patients scheduled for elective shoulder athroscopy. The patients randomise themselves by choosing the type of anesthesia technique (general anesthesia or interscalene block) after detailed description of both techniques. They receive the standard, routine medical care (monitoring and anesthesia techniques) during which the obtained data of arterial pressure, heart rate, peripheral and cerebral oxygen saturation will be statistically analysed and compared.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Impaired Oxygen Delivery Cerebral Hypoxia

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: Inclusion criterion for the study was the approval for surgery under general or regional anesthesia with ASA I and ASA II patients classification. - Exclusion Criteria: * The patients who have refused to take part in the study, patients assessed as ASA III or higher, who have cerebrovascular or coronary disease, coagulopathy, hypersensitivity to local anesthetics or other contraindications to one or the other type of anesthetic techniques All patients in whom the operation lasted less than 20 minutes or longer than 90 minutes, have been also excluded from the study.

Outcomes

Primary Outcomes

changes in arterial pressure from baseline

Time frame: baseline, during the operation, one hour after the operation

Secondary Outcomes

changes in regional cerebral oxygen saturation from baseline

Time frame: baseline, during the operation, one hour after the operation

Data from ClinicalTrials.gov

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