To check the pain relieving efficacy of dexmedetomidine in above collar bone brachial plexus block (usg guided) when given perineurally versus intravenous dexmedetomidine as an adjuvant to ropivacaine versus when ropivacaine is given alone in adult patients undergoing upper limb surgery

Phase 4

• Conditions: Health Condition 1: O- Medical and Surgical

• Registration Number: CTRI/2020/10/028270
• Lead Sponsor: Dr S N medical college Jodhpur

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

ALL PATIENTS UNDERGOING UPPER LIMB SURGERY OF LESS THAN 2 HRS BETWEEN AGE GROUP OF 18 TO 60 YEARS, BMI BELOW 30, BELONGING TO ASA 1 AND 2 AND HAVING ALL ROUTINE LAB TEST WITHIN NORMAL RANGE WITH FREE FROM ANY ACUTE OR CHRONIC SYSTEMIV ILLNES

Exclusion Criteria

1. ANY PATIENT HAVING HYPERSENSITIVITY OR CONTAINDICATION TO ROPIVACAINE AND DEXMEDETOMODINE.

2. LOCAL PATHOLOGY AT THE SITE OF INJECTION OR DISABILITY LIMITING THE PERFORMANCE OF BLOCK

3. PREGNANT , LACTATING MOTHER, DIABETIC PATIENTS, NEUROLOGICAL DEFICIT IN OPERATIVE LIMB.

4. PATIENT WITH CHRONIC PAIN OR ON LONG TERM ANALGESIC

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Primary Outcome of our study is onset of sensory block, duration of sensory block, duration of analgesia during comparison between analgesic efficacy of Dexmedtomidine as adjuvant to ropivacaine in supraclavicular block (USG guided) when administred perineurally versus intravenous versus when ropivacaine given alone in adult patients undergoing upper limb surgery.Timepoint: VAS Score analysis, BP, heart rate before procedure, at the time of procedure and 24 hrs monitoring of Vitals and duration of sensory and motor block.

Secondary Outcome Measures

Name	Time	Method
Secondary Outcome is onset of motor block, duration of motor block, compare post-operative rescue analgesic (tramadol, diclofenac) consumption in first 24 hours, Any changes inNIBP,PR.SpO2in first 24 hour ,Patientâ??s satisfaction score ,Any complications / adverse effects/side effects of block in term of above mentioned three groups after administering block . <br/ ><br>Timepoint: VAS Score analysis, BP, heart rate before procedure, at the time of procedure and 24 hrs monitoring of Vitals and duration of sensory and motor block.