Comparison of two different drugs as adjuvants to local anesthesia in supraclavicular brachialplexus block for upper limb surgeries
Not Applicable
- Registration Number
- CTRI/2021/05/033452
- Lead Sponsor
- Dr Anitha A
- 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 Anesthesiologist physical status 1 and 2
Exclusion Criteria
Any neurological deficit, peripheral neuropathies, myopathies or
chronic pain in the operative limb.
History of anaphylaxis to local anaesthetics or known allergy to any
of the study drugs to be used.
Any history of bleeding diathesis or coagulation abnormalities.
Any skin infection or local disease at the needle insertion site. BMI more than 35kg/sq-m, failure to achieve adequate block within 30 mins of administration.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time to onset of sensory and motor block. <br/ ><br>Duration of sensory and motor block. <br/ ><br>Duration of analgesiaTimepoint: Time to onset of sensory and motor block. <br/ ><br>Duration of sensory and motor block. <br/ ><br>Duration of analgesia
- Secondary Outcome Measures
Name Time Method Pain scores <br/ ><br>Adverse effects- Hypotension, Bradycardia, <br/ ><br>Tachycardia, Hypoxemia, Sedation, Nausea, <br/ ><br>Vomiting, Pruritis, Skin Rash, Dry mouth, <br/ ><br>DyspneaTimepoint: Pain assessed by Visual Analogue scale <br/ ><br>Hypotension(noninvasive blood pressure less <br/ ><br>than 20% of baseline) <br/ ><br>Bradycardia(heart rate less than 60beats/minute) <br/ ><br>Tachycardia(heart rate more than <br/ ><br>100beats/minute) <br/ ><br>Hypoxemia(oxygen saturation less than 90%) <br/ ><br>Sedation assessed by Modified Ramsay <br/ ><br>sedation scale <br/ ><br>Nausea and vomiting assessed by Nausea and <br/ ><br>vomiting scale