A clinical trial to comparatively evaluate the analgesic efficacy of ultrasound guided erector spinae plane block versus wound site infiltration in patients undergoing open nephrectomy.
Phase 2
- Conditions
- Health Condition 1: N19- Unspecified kidney failure
- Registration Number
- CTRI/2024/02/062847
- Lead Sponsor
- Dayanand Medical college and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adult patients of 18-75 years of age, American Society of Anaesthesiologists (ASA) I-III undergoing open nephrectomy with flank incision
Exclusion Criteria
1. Patients allergic to local anaesthetics being used
2. Infection at the site of infiltration of local anaesthetic
3. Patients with uncontrolled bleeding diathesis evidenced by history and laboratory investigations
4. Patients with Psychiatric disorder
5. Patients unable to comprehend VAS score
6. Patients with chronic opioid abuse
7. Refusal to participate in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the analgesic efficacy of ESPB and wound site infiltration in open nephrectomy patients in post operative period.Timepoint: Comparative consumption of the total amount of rescue opioid analgesic in a 24 hour period among both the groups will be noted and bidirectional Visual Analogue Scale(VAS) will be recorded at rest and on movement preoperatively i.e prior to block administration before induction of general anesthesia and then postoperatively every hourly for the first 4 hours, 2 hourly for next 2 hours and 4 hourly till 24 hours.
- Secondary Outcome Measures
Name Time Method Duration of analgesia and Quality of revovery questionnareTimepoint: Quality of recovery questionnare at 24 hours postoperatively