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Examining the effectiveness of two different doses of dexamethasone when used as an additive to upper limb nerve block

Not Applicable
Not yet recruiting
Conditions
Health Condition 1: S698- Other specified injuries of wrist,hand and finger(s)Health Condition 2: S599- Unspecified injury of elbow and forearmHealth Condition 3: S499- Unspecified injury of shoulder andupper arm
Registration Number
CTRI/2024/03/064718
Lead Sponsor
Divya Prabhash
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Patients undergoing upper limb surgeries under supraclavicular brachial plexus block.

Exclusion Criteria

1. Patient refusal

2. Neurological deficits involving brachial plexus

3. Patients with diabetes mellitus, hepatic or renal failure

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine onset of sensory blockade with two different doses of dexamethasone as adjuvant to block.Timepoint: In minutes
Secondary Outcome Measures
NameTimeMethod
Onset and Duration of motor blockadeTimepoint: In minutes;Side Effects / ComplicationsTimepoint: (If any);To determine duration of sensory blockade with two different doses of dexamethasone as adjuvant to block.Timepoint: In minutes
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