Post operative pain relief for all upper limb surgeries by comparing two local anaesthetic drugs
Not Applicable
- Conditions
- Health Condition 1: 7- OsteopathicHealth Condition 2: 7- OsteopathicHealth Condition 3: M958- Other specified acquired deformities of musculoskeletal system
- Registration Number
- CTRI/2024/03/063512
- Lead Sponsor
- SREE BALAJI MEDICAL COLLEGE AND HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients receiving 0.25% Levobupivacaine with 1mcg/kg Dexmedetomidine group L
Patients receiving 0.375% Ropivacaine with 1mcg/kg Dexmedetomidine group R
ASA Grade I and II
All age groups
Obese patients
Patients posted for elective surgeries
Exclusion Criteria
ASA III and IV
Known case of hypersensitivity reaction to local anesthetics
Bleeding diathesis and Peripheral neuropathy and neuromuscular disease and psychiatric disorders
Local infection at the site of puncture
Patients with polytrauma
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method It is an observational study to find out whether 0.25% levobupivacaine 1mcg/kg Dexmedetomidine or 0.375% ropivacaine with 1mcg/kg Dexmedetomidine has the early onset of sensory and motor blockade prolonged duration of analgesia and better hemodynamic stabilityTimepoint: 0 hours and 1 hour till 10 hours
- Secondary Outcome Measures
Name Time Method duration of analgesia & to assess better hemodynamic stability.Timepoint: at 30mins 1hour 2hour 3hour