A study to assess post operative pain in a patient of kidney transplant recipient
Not Applicable
Completed
- Conditions
- Health Condition 1: N186- End stage renal disease
- Registration Number
- CTRI/2023/07/054808
- Lead Sponsor
- Post Graduate Institute of Medical Education and Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 52
Inclusion Criteria
All patient undergoing kidney transplant surgery (living donor and cadaveric) aged 18-65 years
Exclusion Criteria
Patient who refuse to give consent
Patient with coagulation disorders
Patient with opioid addiction
Patient who are allergic to local anesthetics
Patient with known psychiatric or mental problems
Patient having local infection of the skin where block is to be given
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare VNRS scores 24 hours post operatively at rest, between continuous erector spinae plane block (CESPB) and continuous epidural infusion (CEI) groupsTimepoint: To compare VNRS scores 24 hours post operatively at rest, between continuous erector spinae plane block (CESPB) and continuous epidural infusion (CEI) groups
- Secondary Outcome Measures
Name Time Method