Postoperative pain relief after leino-renal shunt surgery with continuous infusion of local anaesthetics in the abdominal wall
Not Applicable
- Conditions
- Health Condition 1: null- Patients scheduled to undergo leino-renal shunt surgery
- Registration Number
- CTRI/2014/10/005108
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 20
Inclusion Criteria
ASA I-III patients of age > 18years, undergoing LR shunt surgery will be enrolled in the study
Exclusion Criteria
•Patient refusal
•Age < 18 yrs
•Emergency surgery,
•Known hypersensitivity to local anaesthetics
•Chronic pain conditions
•History of drug abuse
•Inability to understand VAS or PCA functioning
•Severe renal or liver dysfunction
•Morbid obesity
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intravenous patient controlled analgesia(IV PCA) morphine consumptionTimepoint: 24 hrs postoperatively
- Secondary Outcome Measures
Name Time Method Complications or adverse effects such as bleeding/hematoma formation, infection, or local anaesthetic toxicityTimepoint: 24 hrs after surgery;Incidence of opioid related side-effects (nausea/vomiting, sedation, respiratory depression, postoperative ileus)Timepoint: 24 hrs after surgery;Patient satisfaction with the quality of postoperative analgesiaTimepoint: 24 hours after the end of surgery;Postoperative visual analog scale (VAS) scores at rest and on coughingTimepoint: 1, 2, 6, 12, 24, 48, and 72 hours after surgery;Time to first requirement of analgesic doseTimepoint: After the end of surgery <br/ ><br>