COMPARISON OF ULTRASOUND GUIDED TWO DIFFERENT NERVE BLOCKS IN ADULT PATIENTS UNDERGOING SHOULDER SURGERY FOR PAIN RELIEF
Not Applicable
- Conditions
- Health Condition 1: M663- Spontaneous rupture of flexor tendons
- Registration Number
- CTRI/2020/09/027534
- Lead Sponsor
- Vardhaman Mahavir Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adult patients (18-65 yrs) of either sex belonging to American Society of Anaesthesiologists (ASA) Physical Status classification I/II and scheduled for elective unilateral arthroscopic shoulder surgery under general anaesthesia.
Exclusion Criteria
1. Patientâ??s refusal
2. Preexisting respiratory dysfunction.
3. History of cardiac, renal or hepatic disease
4. Preexisting neurologic deficits or neuropathy affecting the brachial plexus
5. Contraindications to the peripheral nerve blocks (eg. Coagulopathy)
•History of known Local Anesthetic allergy
•Patients undergoing revision, planned open, or irrigation and debridement procedures
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the duration of analgesia of two blocks in adult patients undergoing arthroscopic shoulder surgery under general anaesthesiaTimepoint: This is the specific time patient would require pain medication (presses PCA button post surgery for pain with NRS score more than 4)
- Secondary Outcome Measures
Name Time Method diaphragmatic function assessmentTimepoint: 1 hr after block;Morphine consumption via PCA pump postoperativelyTimepoint: 2 hr, 4 hr, 6 hr, 8 hr, 12 hr and 24 hr postblock;NRS pain scoreTimepoint: 2hr, 4 hr, 6 hr, 8 hr, 12 hr and 24 hrs postblock;pulmonary function testTimepoint: 1 hr after block