Comparision of epidural analgesia with transversus abdominis plane block in renal transplant recipients
Not Applicable
Completed
- Conditions
- Health Condition 1: null- End stage renal diseaseHealth Condition 2: N186- End stage renal disease
- Registration Number
- CTRI/2016/12/007577
- Lead Sponsor
- PGIMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 62
Inclusion Criteria
Patients with end stage renal disease scheduled to undergo live donor renal transplant
Exclusion Criteria
1.Refusal to give consent.
2.Derangements of coagulation profile contraindicating the use of epidural anaesthesia (INR of >=1.3 will be considered a cut-off for the study).
3.Addiction to opioids, or alcohol, or history of any other substance abuse.
4.Allergy to local anaesthetic drugs.
5.Extension of surgical incision lateral to anterior axillary line or above T8 dermatome.
6.Inability to communicate (e.g. known psychiatric disorders).
7.Accidental complications such as dural puncture or peritoneal breach.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method