Clinical trial to assess the efficacy of ultrasound guided thoracic paravertebral block in patients who are under going percutaneous kidney stone removal procedures under general anesthesia
Not Applicable
Completed
- Conditions
- Health Condition 1: N200- Calculus of kidneyHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2021/02/031332
- Lead Sponsor
- arayana Medical College and Hospitals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1. Patient aged between 18-60 years.
2 .ASA 1,2 posted for PCNL surgeries under GA.
3.Patients giving informed written consent.
Exclusion Criteria
1. Patient refusal
2. Patient belonging to ASA 3 and 4
3. Local infection
4. Patient with history of drug allergy to local anesthetics.
5. Patients with hemorrhagic diathesis.
6. Patient with coexisting cardiac, pulmonary ,hepatic, renal disorders.
7. Inflammatory /infective skin lesions at the site of giving block.
8. Diseases and deformities of spinal cord
9. Current pregnancy.
10.Depressive illness or anxiety disorders.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual Analog Score <br/ ><br>Time to first Rescue Analgesia <br/ ><br>24 hr Opioid ConsumptionTimepoint: 30 minutes,2 hrs,4hrs,8 hrs,12hrs,24hrs
- Secondary Outcome Measures
Name Time Method 1.Time for first rescue analgesia (IV fentanyl1mcg/kg) <br/ ><br>2.No of rescue analgesics over first 24 hours <br/ ><br>Timepoint: within 24 hours after surgery