TCTR20230916002
Enrolling By Invitation
Phase 3
Comparing the Efficacy of Perioperative Pain Control Between Intravenous Parecoxib and Oral Etoricoxib in ACL Reconstruction: A Randomized Controlled Trial
Faculty of Medicine, Prince of Songkla University0 sites160 target enrollmentSeptember 16, 2023
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Anterior cruciate ligament injury patients which underwent anterior cruciate ligament reconstruction surgery.
- Sponsor
- Faculty of Medicine, Prince of Songkla University
- Enrollment
- 160
- Status
- Enrolling By Invitation
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •The patients diagnosed as anterior cruciate ligament injury aged 18\-50 years old who scheduled for arthroscopic ACLR.
Exclusion Criteria
- •1\. Patient who schedules for bone\-patellar tendon\-bone autograft ACL reconstruction
- •2\. Allergy to acetaminophen, aspirin, sulfonamide, NSAIDs or opioids
- •3\. History of dyspepsia, peptic ulcer, or abnormal bleeding
- •4\. History of ASCVD (History of diagnosis ACS, clinical likely ACS)
- •5\. History of CKD
- •6\. History of asthma or COPD because selective COX\-inhibitor induce spasm
- •7\. History of cerebrovascular disease
- •8\. History of peripheral arterial disease
- •9\. Patients who have Kratom or Marijuana used or substance abuse
- •10\. Patients who anesthesiologist concerns the risk of general anesthesia (GA) is higher than spinal anesthesia; hence, they prefer to use spinal anesthesia rather than general anesthesia
Outcomes
Primary Outcomes
Not specified
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