The effect of intravenous infusion of lidocaine during surgeryon pain and nausea-vomiting in Stomach Bypass with Laparascopy
Phase 2
- Conditions
- Relation between effect of intravenous infusion of lidocaine during and after surgery on pain and nausea-vomiting in Stomach Bypass with Laparascopy.
- Registration Number
- IRCT2015121924754N2
- Lead Sponsor
- Vice chancellor for research, Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 40
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: At zero, half an hour, one and six and twelve and twenty-four hours. Method of measurement: V.A.S.;Nausea-vomiting. Timepoint: At zero, half an hour, one and six and twelve and twenty-four hours. Method of measurement: Asking of patient.;Systolic blood pressure. Timepoint: At time zero, half an hour and one hour after the operation. Method of measurement: Mercury sphygmomanometer.;Diastolic blood pressure. Timepoint: At time zero, half an hour and one hour after the operation. Method of measurement: Mercury sphygmomanometer.;Heart Rate count. Timepoint: At time zero, half an hour and one hour after the operation. Method of measurement: Pulse Rate count.
- Secondary Outcome Measures
Name Time Method