A study to determine effective dose of dexmedetomidine when added to ropivacaine to produce efficient ultrasound guided supraclavicular brachial plexus block in surgeries of arm
Not Applicable
Completed
- Conditions
- Health Condition 1: M80-M85- Disorders of bone density and structure
- Registration Number
- CTRI/2020/02/023167
- Lead Sponsor
- P Akshara
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
Patients undergoing elective upper limb surgeries
American Society of Anaesthesiologist I or II
Exclusion Criteria
Patient refusal
Patients with pre existing peripheral neuropathy of upper limb
Patients allergic to local anesthetics
Patients on adrenoreceptor agonist/ antagonist therapy
American Society of Anaesthesiologist III and above Patients with coagulation disorders
Local site infection
BMI above 30
Poorly controlled Hypertension
Poorly controlled Diabetes mellitus
Severe CVS abnormalities
Renal/Hepatic insufficiency
Pregnancy/ Lactating mothers
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare duration of analgesia of two different doses of dexmedetomidine in terms of first rescue analgesia requirementTimepoint: Post operative period
- Secondary Outcome Measures
Name Time Method Onset and duration of sensorimotor blockade <br/ ><br>Peri operative analgesic requirements <br/ ><br>Sedation <br/ ><br>Hemodynamic stabilityTimepoint: Peri operative Period