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Clinical Trials/CTRI/2019/09/021449
CTRI/2019/09/021449CompletedPhase 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 enrollmentStarted: TBDLast updated:
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Trial Snapshot

Phase
Phase 4
Status
Completed
Sponsor
Enrollment
70
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

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

Investigators

Sponsor
Department of anaesthesiology

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