Comparing pain relief between two different blocks in thoracoscopy procedure
Phase 4
- Conditions
- Health Condition 1: J989- Respiratory disorder, unspecified
- Registration Number
- CTRI/2024/07/071023
- Lead Sponsor
- Rajarajeswari Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA 1, 2 and 3 patients of either sex
2. Patients aged between 20 to 70 years
3. Patients undergoing thoracoscopic procedure
Exclusion Criteria
1. Patient’s refusal
2. ASA 4 patients
3. Patients with known hypersensitivity to local anaesthetics
4. Patients with bleeding disorder
5. Patients with epilepsy
6. Mentally unstable patients
7. Patients with neurological deficits
8. Infection at local site
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of duration of analgesia between combination of thoracic segmental spinal and erector spinae block versus thoracic segmental spinal and paravertebral block in patients undergoing thoracoscopic proceduresTimepoint: 1,3,5,10,15,30,45,60,90 minutes
- Secondary Outcome Measures
Name Time Method Sensory blockade level <br/ ><br>Changes in hemodynamic parameters intra-operatively <br/ ><br>SpO2 <br/ ><br>Heartrate <br/ ><br>Blood pressure <br/ ><br>Post-operative complications if anyTimepoint: 1,3,5,10,15,30,45 minutes, 1 hour, 1.5 hour for intraoperatively <br/ ><br>1,2,4,6,8,12,24 hours for postoperative monitoring