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Clinical Trials/CTRI/2019/09/021449
CTRI/2019/09/021449
Completed
Phase 4

Comparative study to evaluate propofol and combination of propofol and sevoflurane as maintenance agents in reducing postoperative nausea and vomiting in female patients undergoing laparoscopic surgery

Department of anaesthesiology0 sites70 target enrollmentTBD
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Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Department of anaesthesiology
Enrollment
70
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
March 23, 2020
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Department of anaesthesiology

Eligibility Criteria

Inclusion Criteria

  • •female patients belonging to American society of anaesthesiologists (ASA) physical status I or II, scheduled for laparoscopic surgery and requiring endotracheal intubation will be included in the study

Exclusion Criteria

  • •Patients with:
  • •1\. Obesity (BMI \>30kg/m.m)
  • •2\. history of nausea and vomiting or motion sickness
  • •3\. history of gastro\-esophageal reflux disease
  • •4\. history of anti\-emetic use in last 2 weeks before surgery
  • •5\. history of smoking or alcohol use
  • •6\. refusal to participate in study
  • •will be excluded from the study

Outcomes

Primary Outcomes

Not specified

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