IRCT2015121924754N2CompletedPhase 2
Comparison the effect of intravenous infusion of lidocaine with of 1 mg / kg / h and 2mg/ kg / h on reducing pain and nausea-vomiting after surgery of Stomach Bypass with Laparascopy
Vice chancellor for research, Iran University of Medical Sciences0 sites40 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- Phase 2
- Status
- Completed
- Sponsor
- Enrollment
- 40
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 years to 60 years (—)
- Sex
- All
Inclusion Criteria
- •patient consent, age greater than 18 and less than 60 years; BMI less than 50; ASA equal to or less than 3; Intraoperative lidocaine infusion time up to 4 hours; no sensitivity to lidocaine; no heart diseases; no liver diseases; no kidney diseases; no psychiatric diseases; Avoiding the use of alcohol and drugs addiction
- •Exclusion criteria: Withdraw from the study; Intraoperative lidocaine infusion time more 4 hours; conversion laparoscopy to laparotomy
Exclusion Criteria
- Not provided
Investigators
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