TCTR20190316001
Completed
Phase 1
Comparing the efficacy of perioperative intravenous infusion versus intraperitoneal instillation of local anesthetic in reducing post-operative opioid consumption in laparoscopic cholecystectomy: a randomized double-blind controlled trial
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Total opioid consumption in patients receiving lidocaine IV or IP vs saline in laparoschopic surgeryIncidence of shoulder painTime discharge criteria met
- Sponsor
- Chiang Mai University
- Enrollment
- 162
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •All genders between 18 to 70 years of age with good conscious
- •\- Patients with American Society of Anesthesiologists (ASA) physical status classification of I\-II
- •\- Patients subjected to elective laparoscopic cholecystectomy
- •\- Patients who have given informed consent to participate in this study
Exclusion Criteria
- •\- Patients with BMI \>35 (morbid obesity)
- •\- Patients with suspected CA gallbladder and acute cholecystitis
- •\-Patients with severe obstructive sleep apnea
- •\-Patients with preexisting chronic pain, including those who are currently receiving opioid treatments, and those who received analgesics 24 hours prior to surgery
- •\- Patients with a history of local anesthetic allergy
- •\-Patients with previous abdominal surgeries
- •\- Patients with severe liver, cardiac or renal disease (serum creatinine \>2 mg/dl)
- •\-Patients who are unable to communicate and cooperate to pain assessment
Outcomes
Primary Outcomes
Not specified
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