Regional blocks for patients undergoing thoracic surgeries-DSAPB vs RLB
Not Applicable
- Conditions
- Health Condition 1: J479- Bronchiectasis, uncomplicatedHealth Condition 2: C349- Malignant neoplasm of unspecifiedpart of bronchus or lungHealth Condition 3: O- Medical and Surgical
- Registration Number
- CTRI/2022/12/047952
- Lead Sponsor
- PGIMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) Patients undergoing unilateral posterolateral thoracotomy.
2) American Society of Anaesthesiologists (ASA) I or II.
Exclusion Criteria
1)Patient with anticoagulation or bleeding disorder.
2)Pre-existing block site infection.
3)Allergy to local anaesthetics.
4)History of (H/O) daily consumption of analgesics.
5)H/O opiate abuse.
6)Previous surgery in the thoracic vertebral region.
7)Pre-existing chronic pain or cognitive dysfunction.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the quality of Analgesia based on VAS pain score at rest in the <br/ ><br>postoperative period for 48 hours. <br/ ><br>Timepoint: To assess VAS at 0 1 2 3 4 5 6 9 12 15 18 24 30 36 42 48 hrs in the post operative period. <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1)The total dose of opioids received in the postoperative period (at the first 48 <br/ ><br>hours). <br/ ><br>2)The total dose of opioids received in the intraoperative period. <br/ ><br>3)Time taken for the first dose of rescue analgesia. <br/ ><br>4)Incidence of Nausea and vomiting, block complications.Timepoint: 48 hrs in the post operative period.