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The Efficacy of Ultrasound-Guided Erector Spinae Plane Block for Postoperative Analgesia of Patients Undergoing Laparoscopic Cholecystectomy

Not Applicable
Completed
Conditions
cholelithiasis
postoperative pain
Anaesthesiology - Pain management
Oral 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
NameTimeMethod
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
NameTimeMethod
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]
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