analgesia after shoulder arthroscopy

Not Applicable

Recruiting

• Conditions: Anaesthesia

• Registration Number: PACTR202402842689533

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2024-01-16
• Last Update Posted: 4 March 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

•Patients aged 18–65 years
•American Society of Anesthesiologists (ASA) I or II
•Scheduled for elective unilateral shoulder arthroscopy (rotator cuff repair, bankart repair, superior labral tear from anterior to posterior repair, and/or acromioplasty).

Exclusion Criteria

•Coagulation Or bleeding disorder, anticoagulant therapy
•Cervical disc issues,
•Allergy/sensitivity to local anaesthetics and/or opioids,
•Infection in the block area,
•Contralateral hemidiaphragmatic paralysis, pneumonectomy or vocal cord palsy, severe bronchopulmonary disease, including chronic obstructive pulmonary disease and obstructive sleep apnea.
•Pregnancy or suspected pregnancy, breast feeding mother,
•Body mass index greater than 35 kg/m2,
•Significant psychiatric or cognitive conditions interfering with assessment.
•Unstable coronary artery disease, congestive heart failure, or arrhythmias.
•Pre-existing neurological deficits or neuropathy affecting the brachial plexus. Cognitive or intellectual disability resulting in difficulty communicating with the care givers.
•Pre-existing chronic pain or daily consumption of opioid analgesics.
•Significant renal or hepatic impairment.
•Refusal to participate
•Block failure

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
the time to first postoperative analgesia requirement.