To study the effectiveness of addition of the drug clonidine to the local anesthetic drug ropivacaine for use in ultrasound guided transversus abdominis plane block in adult patients undergoing kidney transplantation surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Adult end stage chronic kidney disease patients undergoing renal transplant surgery
- Registration Number
- CTRI/2017/07/009102
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
Inclusion Criteria
Adult patients undergoing renal transplantation.
Exclusion Criteria
1.Refusal to participate
2.Infection at site of proposed block
3.Hypersensitivity to ropivacaine, clonidine or opioids
4.Inability to understand the functioning and use of Patient Controlled Analgesia (PCA)pump or Visual analogue scale
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post-operative 24 hour intravenous morphine consumptionTimepoint: 0 hour,2 hours, 6 hours, 12 hours, 24 hours in post- operative period
- Secondary Outcome Measures
Name Time Method