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Clinical Trials/IRCT20101211005362N31
IRCT20101211005362N31
Recruiting
Phase 1

Comparison study of the preemptive of the two dose of dexmedetomidine (bolus and infusion) on post operative pain, nausea and vomiting for laparoscopic cholecystectomy

Esfahan University of Medical Sciences0 sites90 target enrollmentTBD
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ConditionsPain, nausea and vomiting.

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Pain, nausea and vomiting.
Sponsor
Esfahan University of Medical Sciences
Enrollment
90
Status
Recruiting
Last Updated
3 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • •patient candidate to be operated laparoscopic cholecystectomy
  • •one and two ASA
  • •age between 18 \- 65 year
  • •Patient consent to participate in the study

Exclusion Criteria

  • •Drug addiction
  • •History of dexmedetomidine allergy
  • •People with a BMI above 30
  • •Use of sleeping pills and analgesics chronically

Outcomes

Primary Outcomes

Not specified

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