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Comparison of duration of analgesic efficacy of Ropivacain given perineurally alone and mixed with dexamethasone and dexamethasone given intravenous in USG guided supraclavicular brachial plexus block.

Not Applicable
Conditions
Health Condition 1: M843- Stress fracture
Registration Number
CTRI/2019/04/018591
Lead Sponsor
Department Of Anaesthesiology and Critical Care
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Body weight 30 to 80 kilograms

2.Patients belonging to ASA 1 and 2

3.Patients undergoing upper limb orthopedic surgeries of less than 3 hours duration

4.All laboratory investigations within normal limits

5.Patients free from any associated acute or chronic systemic illnesses

Exclusion Criteria

1.Uncooperative patients

2.Patients hypersensitive to drugs ropivacaine and dexamethasone

3.Local pathology or deformities at site of block

4.Patients with ASA grade 3 and 4

5.Pregnant with lactating mother diabeic neurological deficiet

6.Patients with chronic pain on analgesics

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time of first rescue analgesic (Duration of analgesia):- min <br/ ><br>Number of times rescue analgesic given in 24 hrs:-1, 2, 3, 4, 5. <br/ ><br>Total dose of tramadol consumption in 24 hrs: mg <br/ ><br>Total dose of diclofenac consumption in 24 hrs: mg <br/ ><br>Timepoint: Time <br/ ><br>Before block <br/ ><br>0 Hour (Just after block) <br/ ><br>2 Hour <br/ ><br>4 Hour <br/ ><br>6 Hour <br/ ><br>8 Hour <br/ ><br>10 Hour <br/ ><br>12 Hour <br/ ><br>14 Hour <br/ ><br>16 Hour <br/ ><br>18 Hour <br/ ><br>20 Hour <br/ ><br>22 Hour <br/ ><br>24 Hour <br/ ><br> <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
1.To compare post-operative rescue analgesic (tramadol) consumption in first 24 hours. <br/ ><br>2.NRS pain scores at rest(NRS-R)& at movement(passive/active)NRS-M of operated upper limb in first 24 hours. <br/ ><br>3.Any changes in NIBP,PR.SpO2in first 24 hours <br/ ><br>4.Patientâ??s satisfaction score. <br/ ><br>5.Any complications / adverse effects/side effects of block. <br/ ><br>Timepoint: Time <br/ ><br>Before block <br/ ><br>0 Hour (Just after block) <br/ ><br>2 Hour <br/ ><br>4 Hour <br/ ><br>6 Hour <br/ ><br>8 Hour <br/ ><br>10 Hour <br/ ><br>12 Hour <br/ ><br>14 Hour <br/ ><br>16 Hour <br/ ><br>18 Hour <br/ ><br>20 Hour <br/ ><br>22 Hour <br/ ><br>24 Hour <br/ ><br> <br/ ><br>
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