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Clinical Trials/IRCT20230506058101N1
IRCT20230506058101N1
Recruiting
Phase 3

Evaluation of the prophylactic effect of dexamethasone and droperidol in comparison with dexamethasone and ginger on nausea and vomiting in patients undergoing laparoscopic cholecystectomy

Arak University of Medical Sciences0 sites152 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Arak University of Medical Sciences
Enrollment
152
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • Candidates for laparoscopic cholecystectomy who will be electively referred to Amir al\-Momenin and Valiasr Arak hospitals
  • Age range between 18\-65 years
  • ASA anesthesia class I, II
  • Candidates for general anesthesia
  • All candidate patients for laparoscopic cholecystectomy who undergo surgery
  • Not being allergic to droperidol and ginger
  • The duration of surgery between 60\-150 minutes

Exclusion Criteria

  • Sensitivity to Droperidol and Ginger

Outcomes

Primary Outcomes

Not specified

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