Comparison of Efficacy of Betamethasone Gel With Lidocaine Gel in Prevention of Post Endotracheal Intubation Sore Throat.

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18-60
SponsorJinnah Postgraduate Medical Centre

About this trial

The goal of this clinical trial is to compare the incidence of postoperative sore throat in adult patients of either gender belonging to ASA I or II ,undergoing endotracheal intubation using betamethasone gel versus lidocaine gel. It aims to determine

1: Difference in efficacy of Betamethasone gel and lidocaine gel in prevention of post operative sore throat after endotracheal intubation.

Patients will be assessed for the presence of a sore throat at 6 hours and 24 hours postoperatively. The severity of the sore throat will be graded using the Post-Operative Sore Throat (POST) score.

Eligibility criteria

Qualifiers

Patients aged 18-60 years

Either gender

ASA I to II

Patients planned for elective surgery under general anesthesia not lasting more than 4 hours.

Disqualifiers

Patients requiring more than 2 attempts for successful intubation

Patients undergoing surgeries of oral cavity or pharynx

Mallampati Score of 3 or 4

Patients with upper respiratory tract infection

Trial design

Treatments tested in this trial

  • Betamethasone dipropionate 0.05%
  • Lidocaine hydrochloride 2%

Treatment groups

60 Participants
are divided into 2 treatment groups

Locations

This trial has no locations