Erector spinae plan block
Not Applicable
Completed
- Conditions
- Postoperative painAnaesthesia
- Registration Number
- PACTR201706002388985
- Lead Sponsor
- Tanta University, Faculty of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
ages 18-65 yrs; body mass index (BMI) of more than 40 kg/m2; ASA physical status II-III undergoing laparoscopic bariatric surgery
Exclusion Criteria
allergy to any of the study drugs: coagulation disorders; psychiatric or uncooperative patients; patients with hepatic or renal dysfunction; Patients with history of uncontrolled respiratory / cardiovascular morbidity; Pregnant ladies
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie the analgesic effects of erector spinae plane block in postoperative pain management?
How does ultrasound-guided erector spinae block compare to epidural analgesia in laparoscopic bariatric surgery outcomes?
Are there specific biomarkers that predict optimal response to erector spinae block in obese surgical patients?
What are the potential adverse events associated with erector spinae block and how are they managed clinically?
What combination analgesic strategies with erector spinae block improve postoperative recovery in bariatric surgery?