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

ConditionsSore Throat Dexmedetomidine Analgesia Tonsillectomy

Trial statusRecruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexFemale

Age3-15

SponsorFayoum University Hospital

About this trial

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.

Eligibility criteria

Qualifiers

Age: Childern between 3:15 years old

American Society of Anesthesiologists(ASA) Physical Status I or II

Elective Tonsillectomy

Disqualifiers

Parents refusal

Presence of preoperative sore throat

Known allergy to the study drug

History of upper respiratory tract infection 2 weeks prior to surgery

Trial design

Treatments tested in this trial

Group D (dexmedetomidine group)
Group L (Lidocaine group)

Treatment groups

70 Participants

are divided into 2 treatment groups

Sponsors and collaborators

Fayoum University Hospital

Lead sponsor

Source ClinicalTrials.gov