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Two different approaches for infraclavicular block

Not Applicable
Conditions
Health Condition 1: O- Medical and Surgical
Registration Number
CTRI/2022/11/047078
Lead Sponsor
Vydehi institute of medical science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Patients with ASA I-II.

BMI < 35 kg/m2

Exclusion Criteria

a) Patients with coagulopathy.

b) Patients with sepsis.

c) Patients with pre-existing neuropathy involving brachial plexus. d) Patients who have undergone prior surgeries of the infraclavicular fossa. e) Patients with localized skin infections of the infraclavicular fossa.

f) Patients with allergy to Local Anesthetics.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To study and compare, <br/ ><br> a) Time to complete Sensory and Motor Block <br/ ><br>b) Duration of post-operative analgesiaTimepoint: 0, 6hr, 12hr ,24hr , 48hr
Secondary Outcome Measures
NameTimeMethod
Hemo-dynamic changes in the intra-operative period b) Adverse effects of costoclavicular or Paracoracoid approach to IBPBTimepoint: 0, 6hr, 12hr, 24hr, 48hr
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