A comparative study to evaluate Perfusion index with two volumes of 0.75% Ropivacaine and 4 milligrams of Dexamethasone
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/07/044159
- Lead Sponsor
- Dr Yoganarasimha
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients willing to give informed consent.
2. ASA physical status I and II patients.
3. Patients undergoing elective upper limb surgery.
4. Patients with BMI of 18 to 30kg/m2
Exclusion Criteria
1. Patients with any contraindications for peripheral nerve block.
2. Patients having a known allergy to the study drug.
3. Patients having peripheral neuropathy, coagulation disorders or local site infection.
4. Patients with Cardiogenic or hypovolemic shock.
5. Patients with Respiratory insufficiency.
6. Emergency upper limb surgeries.
7. Pregnant women.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess, compare and evaluate the Perfusion <br/ ><br>index of the limb before and after achieving <br/ ><br>complete motor block.Timepoint: 0 minutes,2 minutes, 4 minutes, 6 minutes, 8 minutes, 10 minutes,15 minutes, 20 minutes, 25 minutes, 30 minutes
- Secondary Outcome Measures
Name Time Method Overall SafetyTimepoint: 0 minutes,2 minutes, 4 minutes, 6 minutes, 8 minutes, 10 minutes,15 minutes, 20 minutes, 25 minutes, 30 minutes