Postoperative pain relief and incidence of chronic pain in patients undergoing arthroscopic shoulder surgery: comparison between interscalene brachial plexus block and parecoxib plus interscalene brachial plexus block

Phase 4

Recruiting

• Conditions: verbal numberical rating scoreadverse effects; Postoperative pain relief; chronic pain; arthroscopic shoulder surgery; interscalene brachial plexus block; parecoxib

• Registration Number: TCTR20140716001
• Lead Sponsor: Prince of Songkla University

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2014-07-16
• Study Completion: 2015-12-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 86

Inclusion Criteria

Eligible patients are those aged 18 65 years of either sex American Society of Anesthesiologists ASA physical status I II and body mass index BMI between 16 35

Exclusion Criteria

The exclusion criteria are patients who are allergic to sulfonamides or celecoxib with impaired hepatic or renal functions alcohol or substance abuse chronic pain except pain in the shoulder or daily intake of analgesics uncontrolled medical disease hypertension and diabetes mellitus and inability to communicate

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Amout of postoperative PCA morphine consumption medical record

Secondary Outcome Measures

Name	Time	Method
Proportion of chronic pain medical records