MedPath

To compare the amount of drug absorbed when deposited above or below the sheath covering the nerves lies above the collar bone under ultrasound guidance

Phase 4
Conditions
Health Condition 1: null- Patients undergoing elbow or below elbow surgeries
Registration Number
CTRI/2018/01/011539
Lead Sponsor
CIDRF
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

ASA 1 and 2 and weighing 50-60kg patients undergoing elbow or below elbow surgeries

Exclusion Criteria

H/o any co-morbidities, coagulopathy, Local anaesthetic allergy, infection at the site of block, preexisting neurological deficit of the surgical limb

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Peak Plasma ConcentrationTimepoint: Pre block (Baseline), 10, 20, 30, 45, 60, 90, 120 minutes post Brachial plexus block
Secondary Outcome Measures
NameTimeMethod
Complete Motor BlockadeTimepoint: every 3 minutes for first 15 minutes and then every 5 minutes till scale 0 sensory and motor blockade or 40 minutes which ever earlier;Complete Sensory BlockadeTimepoint: every 3 minutes for first 15 minutes and then every 5 minutes till scale 0 sensory and motor blockade or 40 minutes which ever earlier;Duration of analgesiaTimepoint: 2, 4, 6, 24 post-operative hours from time 0 or till sensory level 2 and motor level 2 whichever earlier <br/ ><br>;Time to Peak Plasma ConcentrationTimepoint: Pre block (Baseline), 10, 20, 30, 45, 60, 90, 120 minutes post Brachial plexus block
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