Pain relief in thoracoscopic procedures without loss of consciousness
Phase 4
- Conditions
- Health Condition 1: J869- Pyothorax without fistula
- Registration Number
- CTRI/2024/08/071781
- 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 60 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 To investigate the analgesic efficacy of combined thoracic segmental spinal anaesthesia and erector spinae plane 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>Heart rate <br/ ><br>Blood pressure <br/ ><br>Patient recovery and satisfaction <br/ ><br>Post-operative complications if anyTimepoint: Intraoperatively, 1,2,4,6,8,12,24 hours