clinical trial to study analgesic efficacy of external oblique fascial plane block in postoperative patients
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/04/051315
- Lead Sponsor
- gopal krishan jalwal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients of either sex in the age group of 18 to 70 years with physical status ASA1 or ASA II
Exclusion Criteria
Consent refusal, Allergic history to local anaesthetic, abnormal coagulation profile, emergency surgeries, contraindications to regional anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the time to first analgesic request postoperatively.Timepoint: 1 year
- Secondary Outcome Measures
Name Time Method 1) NRS Scores, PONV scores, Pruritus, Sedation, respiratory depression, total dose of fentanyl used in 24 hour postoperatively <br/ ><br>2) complications related to blockTimepoint: 1 year