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Comparison of two doses of Dexamethasone in nerve block for relieving pain following arm surgery.

Not Applicable
Conditions
Health Condition 1: S529- Unspecified fracture of forearm
Registration Number
CTRI/2020/09/027929
Lead Sponsor
Department of Anaesthesiology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Patients belonging to ASA I and II Mallampati grade 1 and 2 posted for upper limb surgeries

Exclusion Criteria

Coagulopathies (INR >1.5)

Infection at site of block

A compromised lung function at opposite side of block like pneumothorax hemothorax pneumonectomy

Hypersensitivity to Local anaesthetics or Dexamethasone

Patients refusal or inability to communicate

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Duration of effective post operative analgesiaTimepoint: 24 hours post operative period
Secondary Outcome Measures
NameTimeMethod
Duration of sensory and motor blockTimepoint: 24 hours post operative period;Incidence of post operative nausea vomitingTimepoint: 24 hours post operative period;Rate of infection neurologic complication hyperglycemiaTimepoint: 24 hours post operative period;Time of onset of sensory and motor block <br/ ><br> <br/ ><br>Timepoint: 24 hours post operative period;VAS scoreTimepoint: 24 hours post operative period
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