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RECRUITING
NCT07780760
NA

Effect of Preoprative Nebulized Dexmedetomidine Compared to Nebulized Lidocaine in Attenuating Sore Throat Following Tonsillectomy In Childern.

Sponsor: Fayoum University Hospital

View on ClinicalTrials.gov

Summary

The aim of the study is to compare the effect of nebulized Dexmedetomidine compared to nebulized Lidocaine on postoperative sore throat in childern undergoing Tonsillectomy.

Official title: Effect of Preoprative Nebulized Dexmedetomidine Compared to Nebulized Lidocaine in Attenuating Sore Throat Following Tonsillectomy In Childern. A Prospective, Randomized, Double-Blinded Trial.

Key Details

Gender

FEMALE

Age Range

3 Years - 15 Years

Study Type

INTERVENTIONAL

Enrollment

70

Start Date

2026-09-01

Completion Date

2027-02-01

Last Updated

2026-08-21

Healthy Volunteers

No

Interventions

DRUG

Group D (dexmedetomidine group)

group D (Dexmedetomidine group) will recieve a dose of 1 mcg/kg

DRUG

Group L (Lidocaine group)

will recieve Lidocaine 2%, 1 mg/kg

Locations (1)

Fayoum university Hospitl

Al Fayyum, Egypt