perioperative Analgesic Effect of Erector Spinae Plane Blocks in Whipple Surgery.
Phase 4
Recruiting
- Conditions
- Anaesthesia
- Registration Number
- PACTR202306801227223
- Lead Sponsor
- natioanl liver institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Patients aged 18 to 65 years of both sexes candidate for Whipple operation and classified by American Society of Anesthesiologists (ASA) II and III with Body-mass index of less than 40 kg/m².
Exclusion Criteria
-Pre-existing signi?cant cardiac dysfunction, respiratory, renal or cerebrovascular diseases.
-Patients allergic to any of the study drugs, with opioid addiction or alcohol abuse.
-Body-mass index higher than 40 kg/m².
-Contraindications for neuroaxial block (e.g. Coagulopathy).
-Patients unwilling to participate in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To study the impact of ESP Block on hemodynamic stability and maintenance of intra-operative Analgesia Nociception Index (ANI) accepted range.
- Secondary Outcome Measures
Name Time Method To evaluate the postoperative pain by visual analogue score (VAS), total opioid requirements and incidence of post-operative complications (as measured by the comprehensive complication index (CCI)) within 48 hours.