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Clinical Trials/IRCT20131228015963N10
IRCT20131228015963N10
Recruiting
Phase 3

Comparison of the effect of different doses of intravenous dextrose solution administered intraoperatively on incidence and severity of postoperative nausea and vomiting in patients undergoing rhinoplasty surgery (A randomized controlled trial)

Rasht University of Medical Sciences0 sites144 target enrollmentTBD
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ConditionsPostoperative nausea and vomiting.???? ? ??????? ??? ?? ??? (Postoperative nausea and vomiting)R11.2

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Postoperative nausea and vomiting.
Sponsor
Rasht University of Medical Sciences
Enrollment
144
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Rasht University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • •Female patients aged 18 to 65 undergoing rhinoplasty
  • •Patients who are candidates for rhinoplasty surgery
  • •Patients in ASA ? and ASA ? class

Exclusion Criteria

  • •History of diabetes mellitus (DM)
  • •Known congestive heart failure (CHF)
  • •Pregnant women
  • •Recent opioid use (within 48 hours before surgery)
  • •Having a history of postoperative nausea and vomiting (PONV) or motion sickness
  • •Smoker patients
  • •Known renal or hepatic failure or impaired preoperative tests
  • •Patients who have used anti\-nausea medication 24 hours before surgery.
  • •Patients who have abnormal blood sugar on the morning of surgery. (Blood sugar more than 125 mg/dL)
  • •Known sensitivity to anesthetics used in the study

Outcomes

Primary Outcomes

Not specified

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