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Clinical Trials/IRCT20200825048515N7
IRCT20200825048515N7RecruitingPhase 2

Preventive effect of intravenous dexamethasone on nausea, vomiting and pain after laparoscopic ovarian cystectomy

Esfahan University of Medical Sciences0 sites88 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Recruiting
Enrollment
88

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 65 years (—)
Sex
Female

Inclusion Criteria

  • Being candidate for laparoscopic cystectomy
  • ASA score of 2 according to American Society of Anesthesiologists Classification (ASA class)
  • Informed consent to participate in the study

Exclusion Criteria

  • Contraindications to use of dexamethasone
  • Having severe and uncontrolled diseases of cardiovascular, renal, hepatic, chronic respiratory
  • Taking anti-nausea drugs and painkillers 24 hours before surgery
  • People with a history of gastrointestinal problems and postoperative nausea
  • Having a history of corticosteroids
  • BMI>30 kg/m2
  • Pregnant and elderly women

Investigators

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