Postoperative pain and Anesthesia
Conditions
Interventions
This is a two-arm, double-blind, randomized controlled clinical trial. 92 patients will be included in the study following the inclusion and exclusion criteria. The anesthetic technique used in this s
Sponsors
Hospital São Domingos
Hospital São Domingos
Eligibility
Age
18 Years to 80 Years
Inclusion criteria
Inclusion criteria: Age between 18 and 80 years, of both sexes, with an ASA score (American Society of Anesthesiologists) of 1 to 3, body mass index (BMI) between 20 and 35kg/m² undergoing elective arthroscopic shoulder surgery
Exclusion criteria
Exclusion criteria: Patients will be excluded from the study if they are unable to consent to the study, have neuropsychiatric diseases, cognitive impairment or altered mental status, pre-existing pulmonary disease (obstructive or restrictive), coagulopathy, sepsis, hepatic or renal failure (glomerular filtration rate less than 30ml/min), pregnancy, known or suspected allergy to medications used during anesthesia, chronic pain condition requiring the ingestion of opioids at home and previous surgery in the neck or infraclavicular region ipsilateral to the operated limb
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that patients in the costoclavicular brachial plexus block group will obtain analgesia similar to patients in the interscalene brachial plexus block group, in addition to having a significantly lower prevalence of diaphragmatic paralysis | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected that patients in the costoclavicular brachial plexus block group will have a significantly lower prevalence of diaphragmatic paralysis than patients undergoing interscalene brachial plexus block. | — |
Countries
Brazil
Contacts
Public ContactHiago Parreão Braga Braga
Hospital São Domingos
Outcome results
None listed