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Clinical Trials/CTRI/2024/05/068021
CTRI/2024/05/068021
Not yet recruiting
Phase 4

A prospective randomized double blinded study - Effect of combined paracetamol and dexamethasone on post operative nausea and vomiting. - NI

akshmi Priya R0 sites0 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
akshmi Priya R
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
akshmi Priya R

Eligibility Criteria

Inclusion Criteria

  • 1\. ASA 1 to 2
  • 2\. All Elective FESS surgery
  • 3\. All procedures done under General anaesthesia with a duration of less than 3 hours
  • 4\. Willingness to participate in the study

Exclusion Criteria

  • 1\. Patient’s refusal to give consent
  • 2\. Allergy to paracetamol, ondansetron
  • 3\. Emergency cases
  • 4\. ASA 3 and above
  • 5\. Patients requiring admission to the intensive care unit or
  • mechanical ventilation
  • 6\. Surgery duration more than 3 hours
  • 7\. Patients with history of gastroesophageal reflux disorder, peptic
  • ulcer disease, inflammatory bowel disease.
  • 8\. Patients with history of PONV, systemic diseases with nausea and

Outcomes

Primary Outcomes

Not specified

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