costoclavicular block

Not Applicable

Recruiting

• Conditions: Not Applicable

• Registration Number: KCT0002376
• Lead Sponsor: The Catholic University of Korea, Daejeon St. Mary's Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 11 March 2019

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 70

Inclusion Criteria

American society of anesthesiology (ASA) physical status 1, 2, 3
Age: 19-80 yrs
Patients undergoing shoulder arthroscopic surgery

Exclusion Criteria

Clinically significant coagulopathy
Infection at the injection site
Allergy to local anesthetics
Severe cardiopulmonary disease(American society of anesthesiology (ASA) physical status =4)
Body mass index > 35
Diabetic or other neuropathies
Patients receiving opioids for chronic analgesic therapy
Patients who have refused intravenous patient controlled analgesia (PCA)
Inability to comprehend visual analogue scale (VAS) score and patient controlled analgesia (PCA) device
Patient who does not want to receive costoclavicular or interscalene block
Patients who want to receive a costoclavicular or interscalene block

Study & Design

• Study Type: Interventional Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Diaphragmatic paralysis;Assessment of pulmonary function

Secondary Outcome Measures

Name	Time	Method
Amount of opioid consumption;postoperative pain