Study is to compare efficacy of two different approaches that block the brachial plexus to see the motor and sensory blockade and to assess the tourniquet pain.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/04/032547
- Lead Sponsor
- at KLEs Dr Prabhakar Kore charitable Hospital and Medical Research Centre
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American Society of Anaesthesiologist(ASA) physical status I to II
Age between 18 to 60 years.
Patients undergoing elective surgeries of upper limb under Ultrasound guided Supraclavicular or Infraclavicular Brachial plexus block.
Patients with BMI less than 30.
Provides Consent.
Exclusion Criteria
Patients undergoing emergency surgeries.
Patients with coexisting lung diseases, pregnancy.
Allergy to Local Anaesthetics
Chest deformities
Previous Clavicular fractures.
Neurological deformities.
Patients who do not fulfill inclusion criteria
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of sensory and motor blockade in terminal nerves of brachial plexus and tourniquet pain in ultrasound guided supraclavicular and infraclavicular brachial plexusTimepoint: Baseline after 10 mins half an hour and every 10mins till the end of surgery
- Secondary Outcome Measures
Name Time Method Comparison of duration of block,block performance time and intraoperative and postoperative complications in ultrasound guided supraclavicular and infraclavicular block.Timepoint: Duration of motor and sensory blockade is seen