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Clinical Trials/CTRI/2019/02/017541
CTRI/2019/02/017541
Recruiting
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 enrollmentTBD
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ConditionsHealth Condition 1: K802- Calculus of gallbladder without cholecystitisHealth Condition 2: K802- Calculus of gallbladder without cholecystitis

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: K802- Calculus of gallbladder without cholecystitisHealth Condition 2: K802- Calculus of gallbladder without cholecystitis
Sponsor
Safdarjung Hospital
Status
Recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

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

Outcomes

Primary Outcomes

Not specified

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