The Efficacy of Ultrasound-Guided Erector Spinae Plane Block for Postoperative Analgesia of Patients Undergoing Laparoscopic Cholecystectomy
Not Applicable
Completed
- Conditions
- cholelithiasispostoperative painAnaesthesiology - Pain managementOral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
- Registration Number
- ACTRN12618001106224
- Lead Sponsor
- Basak ALTIPARMAK
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 41
Inclusion Criteria
The patients between 18-70 years of age with ASA status I-II, and scheduled for an elective laparoscopic cholecystectomy surgery,
Exclusion Criteria
The patients with coagulation disorder, known allergy to local anesthetics, infection at the injection site, advanced hepatic or renal failure, chronic opioid consumption and morbid obesity (body mass index over 35 kg m-2)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the postoperative opioid consumption in the first 24 hours by calculating the tramadol dose administered by patient controlled analgesia device.[At the postoperative 24th hour ]
- Secondary Outcome Measures
Name Time Method To assess intraoperative fentanyl consumption by using data-linkage to surgical records[At the end of each surgery ];To assess shoulder pain of the patients by directly asking the patients to rate their pain with a 3-points scale (0=no pain, 1=mild, 2=severe pain)[At the postoperative 15th minute, 30th minute, 60th minute (secondary time-point), 12th hour, 24th hour];To assess pain scores of the patients by using 11-points numerical rating scale (NRS) at the postoperative 15th minute, 30th minute, 60th minute (secondary time-point), 12th hour and 24th hour[at the postoperative 15th minute, 30th minute, 60th minute (secondary time-point), 12th hour and 24th hour]