Comparing two different approaches of Thoracic Paravertebral Block for pain management after surgery
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/09/057638
- Lead Sponsor
- Swarnika Singh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American Society of Anesthesiologists (ASA) physical status I to III
able to give informed consent
able to cooperate with the study process
Exclusion Criteria
history of allergy to local anesthetics.
coagulation disorders.
neurological deficits.
undergone previous thoracotomy.
not provide written informed consent.
severe respiratory dysfunction, hemodynamic instability, or other serious medical conditions.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Rescue analgesic required in 24 hoursTimepoint: Rescue analgesic required in 24 hours
- Secondary Outcome Measures
Name Time Method •The ability to achieve a sensory block in the targeted dermatomes <br/ ><br>•The duration of sensory block <br/ ><br>•VAS score at 0, 4, 8, 12 & 24 hours <br/ ><br>Timepoint: 0H 4H 8H 12H 24H