â??Comparison of low dose additives to local anaesthetic in ultrasound guided upper limb block.â??
Not Applicable
Completed
- Conditions
- Health Condition 1: null- ASA 1 & 2
- Registration Number
- CTRI/2018/02/011669
- Lead Sponsor
- Dr spurthi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1 Adults aged 18 to 55 years undergoing elective and emergency upper limb surgical procedures under supraclavicular brachial plexus block
2 Weight range 40 to 80 kg
3 Adults belonging to either sex of ASA physical status Grade I and II
Exclusion Criteria
1 Patient refusal
2 Patients with pre existing neurological disorders like peripheral neuropathy or motor weakness
3 Known history of hypersensitivity to drugs used
4 History of significant cardiac respiratory renal hepatic or central nervous system diseases
5 Inadequate block
6 Infection at the site of the block
7 History of coagulopathy or anticoagulant medication intake
8 Pregnant or lactating women
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1 To compare the onset of sensory and motor blockade <br/ ><br>2 To compare the duration of sensory and motor blockadeTimepoint: 24 hours
- Secondary Outcome Measures
Name Time Method Secondary objective <br/ ><br>3 To evaluate the adverse effects of low dose adjuvants if any <br/ ><br>4 To compare sedation scoresTimepoint: 24 hours