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Efficacy of erector spinae plane block in relieving the post operative pain of patients undergoing percutaneous nephrolithotomy

Phase 3
Conditions
Health Condition 1: N200- Calculus of kidney
Registration Number
CTRI/2019/04/018477
Lead Sponsor
Department of anaesthesia and intensive care
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1. American society of anaesthesiologists (ASA) physical status I-II

2. Age 18-65 years

3. BMI >18.5 to >25

4. Patient undergoing Percutaneous nephrolithotomy

Exclusion Criteria

1. History of relevant drug allergy

2. Patient refusal

3. History of psychiatric illness, substance abuse or medical therapies resulting in tolerance to opioids

4.Severe cardiovascular, respiratory, metabolic or neurologic disease.

5. Pregnancy

6. Untreated sepsis

7. Local infection

8. Severe coagulopathy (PTI <70% / INR >1.5)

9. Complex stone with anticipation of requiring >1 access site.

10. Prior diagnosis of chronic pain requiring daily opioid analgesic for >1 month prior to diagnosis of

nephrolithiasis.

11. Back or other musculoskeletal deformity that contributes to inaccuracy of the block placement.

12. Fibromyalgia

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the reduction in pain intensity up to 24 hours in post-operative period by the use of visual analogue scale in patients receiving erector spinae plane block after percutaneous nephrolithotomy.Timepoint: 10 mins, 30 mins, 1hr, 4hrs, 8 hrs, 12hrs, 24hrs
Secondary Outcome Measures
NameTimeMethod
To calculate and compare the total dose of antiemetics over 24 in erector spinae plane block group as well as control groupTimepoint: 10 mins, 30 mins, 1hr, 4hr, 8hr, 12hr, 24hr;To calculate and compare the total opioid consumption over 24 hours in erector spinae plane block group as well as control groupTimepoint: 24 hrs;To note any side effects pertaining to the procedure or the drugs used in the present studyTimepoint: 10 mins, 30 mins, 1hr, 4hrs, 8hrs, 12hrs, 24hrs
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