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Clinical Trials/IRCT2015121924754N2
IRCT2015121924754N2
Completed
Phase 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 enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Relation between effect of intravenous infusion of lidocaine during and after surgery on pain and nausea-vomiting in Stomach Bypass with Laparascopy.
Sponsor
Vice chancellor for research, Iran University of Medical Sciences
Enrollment
40
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
8 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Vice chancellor for research, Iran University of Medical Sciences

Eligibility Criteria

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

Outcomes

Primary Outcomes

Not specified

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