To Compare Dexamethasone And Fentanyl As An Adjuvant To 0.5% Bupivacaine And 2% Lignocaine In Supraclavicular Block Under Sonographic Guidance In Upper Extremity Surgeries
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2021/07/034941
- Lead Sponsor
- Shilpa Sarang Kore
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 66
Inclusion Criteria
ASA grade I or II of either sex,
Patients undergoing elective upper limb surgeries
Haemodynamically stable patients with all routine investigations within normal limits
Availability of informed consent.
Exclusion Criteria
Patient refusal
Patients with ASA physical status III and more,
Non cooperative patient
Patients with nerve injury
Patients who have known allergies to any test drugs.
Patients with coagulation disorders or anti coagulant drugs,
Patients with cardiac disease,
Patients with respiratory diseases.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method VAS Score for pain 0. <br/ ><br>Sensory blockade <br/ ><br>Motor blockade <br/ ><br>Duration of sensory blockade <br/ ><br>Duration of motor blockadeTimepoint: VAS Score for pain 0. <br/ ><br>Every 5 minutes from administration of block
- Secondary Outcome Measures
Name Time Method duration of analgesiaTimepoint: 12 hours