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Clinical Trials/CTRI/2019/02/017541
CTRI/2019/02/017541Recruiting未知

Comparative evaluation of preoperative paracetamol and a combination of paracetamol with nebulised or intravenous dexamethasone for prevention of postoperative sore throat

Safdarjung Hospital0 sites0 target enrollmentStarted: TBDLast updated:
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Trial Snapshot

Phase
未知
Status
Recruiting
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • •1. Patients fulfilling the criteria of American Society of Anesthesiologists Physical Status I and II adults
  • •2. scheduled for elective laparoscopic cholecystectomy under general anaesthesia with tracheal intubation.
  • •3. Either gender, aged 18-65 years

Exclusion Criteria

  • •1. Patients with a history of recent respiratory tract infection or sore throat within <2 weeks
  • •2. Patients with anticipated difficult intubation
  • •3. Patients receiving analgesic or steroid therapy or known allergy to study drugs
  • •4. Patients with diabetes, obesity, cardiac, respiratory, hepatic or renal disease
  • •5. Pregnant women
  • •6. Surgery duration greater than 3 hours

Investigators

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To compare a drug (paracetamol) with... | Clinical Trial