TCTR20230724009Not yet recruitingPhase 2
Efficacy of local infiltration anesthesia versus interscalene brachial plexus block for postoperative pain controlled after arthroscopic rotator cuff surgery: A non-inferiority trial
Research Affairs, Faculty of Medicine, Khon Kaen University0 sites56 target enrollmentStarted: July 24, 2023Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 2
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 56
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 Years to N/A (No limit) (—)
- Sex
- All
Inclusion Criteria
- •1. The patients who are required for arthroscopic rotator cuff surgery; which are including arthroscopic examination, rotator interval release, subacromial decompression, limited acromioplasty, arthroscopic rotator repair or debridement for routine and consider performing biceps tenotomy or tenodesis if the patients have biceps tendon lesion
- •2. Aged over 18 years old
- •3. American Society of Anesthesiologists (ASA) physical state I-III
Exclusion Criteria
- •1. Taking opioids for more than 1 month before surgery (chronic opioid used)
- •2. Pre-existing neuropathy at the affected limb
- •3. History of previous surgery of ipsilateral shoulder
- •4. Allergy to study drugs; bupivacaine, adrenaline, ketorolac, TXA, opioids, NSAIDs or paracetamol
- •5. Contraindication to ISB; COPD, skin disease, contralateral lung pathology
- •6. Infection at the site of application
- •7. Bleeding diathesis; coagulopathy, thrombocytopenia
- •8. Inability to understand how to report pain scores
- •9. Inability to understand how to use intravenous PCA
Investigators
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