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.
- 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
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
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
Name Time Method 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
Name Time Method 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>