Comparison between intraperitoneal versus transversus abdominis plane block by ropivacaine for postoperative analgesia in laparoscopic cholecystectomy
Phase 2
Recruiting
- Conditions
- laparoscopic cholecystectomy.
- Registration Number
- IRCT20190511043550N4
- Lead Sponsor
- Shiraz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 68
Inclusion Criteria
Obtaining informed consent
Patient aged 18 to 65 years with ASA class I & II who is a candidate for laparoscopic cholecystectomy
Exclusion Criteria
Conductive heart diseases that prevent the use of local anesthetics.
Patients taking painkillers for other chronic pain
Patients with a history of drug use or alcoholism
BMI> 35
Patients who are unable to express pain score for any psychological reason
Previous abdominal surgery
Allergy to any local anesthetic
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Post operative pain. Timepoint: The patient's pain is measured at 0, 2, 4, 8, 12, 18 and 24. Method of measurement: The patient's pain is measured, and recorded by the recovery staff based on the VAS criteria or scoring of pain sensation and by the ward staff after discharge from the recovery.
- Secondary Outcome Measures
Name Time Method