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

• Register: TCTR
• Last refreshed on: 29 April 2024
• Main ID: TCTR20140716001
• Date of registration: 16/07/2014
• Prospective Registration: No
• Primary sponsor: Prince of Songkla University
• Public title: 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
• Scientific title: 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
• Date of first enrolment: 04/03/2013
• Target sample size: 86
• Recruitment status: Recruiting
• URL: https://www.thaiclinicaltrials.org/show/TCTR20140716001
• Study type: Interventional
• Study design: Randomized
• Phase: Phase 4

Countries of recruitment

Thailand

Contacts

• Name: Sasikaan - Nimmaanrat
• Affiliation: Prince of Songkla University

• Name: Sasikaan - Nimmaanrat
• Affiliation: Prince of Songkla University

Key inclusion & exclusion criteria

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













Age minimum: 18 Years
Age maximum: 65 Years
Gender: Both

Health Condition(s) or Problem(s) studied

Postoperative pain relief
chronic pain
arthroscopic shoulder surgery
interscalene brachial plexus block
parecoxib

verbal numberical rating score adverse effects
Postoperative pain relief
chronic pain
arthroscopic shoulder surgery
interscalene brachial plexus block
parecoxib

Intervention(s)

patients in this arm will receive paracoxib 40 mg iv 1-2 hrs before operation and another 40 mg after the first dose,patients in this arm will receive NSS 2 ml iv 1-2 hrs before operation and another 2 ml after the first dose

parecoxib,placebo

Experimental Drug,Placebo Comparator No treatment

Primary Outcome(s)

Amout of postoperative PCA morphine consumption medical record

Secondary Outcome(s)

Proportion of chronic pain medical records

Secondary ID(s)

Prince of Songkla Un

Source(s) of Monetary Support

Prince of Songkla University

Secondary Sponsor(s)

Prince of Songkla University

Ethics review

Status: Submitted, approved
Approval date:
Contact:

Faculty of Medicine

Results

• Date Completed: 31/12/2015