An study to evaluate the requirement of post operative pain medication in patients undergoing thoracic surgeries if ultrasound guided serratus plane block and erector spinae plane block was give
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/07/055040
- Lead Sponsor
- A
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA Grade I and II
Primary Unilateral Thoracic Surgery
BMI 20-36
Weight higher than or equal to 50 Kg
Exclusion Criteria
Patient Refusal or not giving Consent
ASA grade >II
Pregnant Patients
Pre-existing neurological disorder
Chronic Opiod Use
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method â?¢To evaluate post operative analgesia after administering erector spinae plane block (ESPB) and Serratus anterior plane block (SAPB) in patients undergoing thoracic surgeries using numerical rating scale (NRS) score.Timepoint: At the time of extubation, 2,4,6,8,12,16,24 hour
- Secondary Outcome Measures
Name Time Method â?¢To observe the need of add on analgesia (Intra op and post op opioids) <br/ ><br>â?¢To evaluate overall duration of analgesia after thoracic surgeries. <br/ ><br>â?¢To observe post operative pulmonary functions. <br/ ><br>â?¢To observe the occurrence of adverse effects, if anyTimepoint: At the time of extubation, 2,4,6,8,12,16,24 hour