A Study Comparing the Efficacy of three different doses of Magnesium Sulphate as Adjuvant to Ropivacaine for Supraclavicular Brachial plexus block
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1,Patient undergoing elective upper limb surgeries,
2,Age 18-60 years
3,Body weight 45-75kg
4,ASA I and II
Exclusion Criteria
1,Patient Refusal
2,Age <18years and age >65 years.
3,pregnant Women
4,ASA III and above
5,infection at the site of block
6,H/O allergy to local anesthetic drugs.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Onset of sensory and motor blockade following administration of supraclavicular block.Timepoint: The onset and degree of sensory and motor block will be observed and recorded for the first 30 mins in every 5 minute interval.
- Secondary Outcome Measures
Name Time Method Compare the hemodynamic changes, Nausea, Vomiting, Pruritis.Timepoint: Outcome is assessed immediately after surgery and up to 24 hours after surgery.