TCTR20240708004
Not yet recruiting
Phase 3
Efficacy of intravenous lidocaine infusion for postoperative quality of recovery in laparoscopic gynecological surgery : A triple-blind, randomized controlled trial
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Quality of recoveryPostoperative painPostoperative nausea and vomiting
- Sponsor
- Rajavithi Hospital
- Enrollment
- 64
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Patients who scheduled for elective laparoscopic gynecological surgery for benign diseases
- •2\. ASA physical status 1\-2
Exclusion Criteria
- •1\. Pregnancy
- •2\. Body weight \< 40 kg or BMI \> 35 kg/m2
- •3\. History of local anesthetic allergy
- •4\. History of cardiac arrhythmia
- •5\. Cirrhosis or elevated AST or ALT \>/\= 2x of normal upper limit
- •6\. GFR \</\= 60 ml/min/1\.73m2
- •7\. Neurological disease
- •8\. NSAID or sulfa drugs allergy
- •9\. History of GI bleeding or peptic ulcer
- •10\. Regular use of analgesics
Outcomes
Primary Outcomes
Not specified
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