A comparison of two additive drugs to conventional local anesthesia in patients undergoing upper limb surgeries under regional anaesthesia.
Phase 2
- Conditions
- Health Condition 1: M00-M99- Diseases of the musculoskeletal system and connective tissueHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2023/08/056862
- Lead Sponsor
- DEPARTMENT OF ANAESTHESIOLOGY AND CRITICAL CAREINSTITUTE OF NAVAL MEDICINE INHS ASVINI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA Grade I & II
Patient undergoing upper limb orthopaedic surgeries
Exclusion Criteria
1.Patients are unwilling
2.Patients with bleeding disorders,
3.Patients on anticoagulants,
4.Patients with neurological and musculoskeletal disease,
5.Infection at the site of injection
6.History of allergy to local anaesthetics
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare:- <br/ ><br>(a)The onset of sensory and motor blockade. <br/ ><br>(b)The duration of sensory and motor blockade. <br/ ><br>Timepoint: (a)Immediately after positioning the patient supine and every 5 minutes to check for onset of sensory and motor blockade <br/ ><br>(b)In the post operative period NRS score for pain, SpO2, sensory and motor weakness, requirement of rescue analgesia, will be noted during following intervals: 0-2 hours, 4-6 hours, 6-12 hours, 12-24 hours.
- Secondary Outcome Measures
Name Time Method Intraop & post op side effects & complications <br/ ><br>Timepoint: Immediately after positioning of patient uptil the surgery is finished. <br/ ><br>In the post operative period, Basal hemodynamics (HR, NIBP) & SpO2, requirement of rescue analgesia, nausea, vomiting will be noted during following intervals: 0-2 hours, 4-6 hours, 6-12 hours, 12-24 hours.