Post operative analgesic consumption with or without sono-guided Erector Spinae Plane Block in patients undergoing abdominal surgery: A randomised, controlled, interventional study.
Phase 1
- Registration Number
- CTRI/2021/02/030907
- Lead Sponsor
- Dept of Anaesthesiology SMS Medical College and Attached Group of Hospitals
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients belonging to American Society of Anesthesiologists (ASA):
Grade I: Without co-morbid conditions
Grade II: Controlled co-morbid conditions
Grade III : Poorly controlled co-morbid conditions
2.Weight 40-80 kg
Exclusion Criteria
1.Patients not willing to participate in the study
2.H/O allergic reactions to local anesthetics
3.Patients on anticoagulant therapy and H/O coagulation disorders
4.Local infection at the proposed site of puncture for Erector Spinae Plane block
5.Chronic use of opioids or corticosteroids.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the difference in mean analgesic dose required post operative period in both groupsTimepoint: 12 hours and 24 hours
- Secondary Outcome Measures
Name Time Method To determine the time of first rescue analgesic in both groups.Timepoint: 12 hours , and every 1 hour thereafter upto 24 hours.