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Clinical Trials in Egypt / NCT07780760
Recruiting Not applicable

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

NCT07780760 · tracked via the Priya Life Science Egypt tracker
Sponsor
Fayoum University Hospital
Phase
Not applicable
Started
2026-09-01
Last updated
2026-08-21

Condition(s) studied

Sore ThroatDexmedetomidine AnalgesiaTonsillectomy

Investigational drug(s) / intervention(s)

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

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

Group L (Lidocaine group): will recieve Lidocaine 2%, 1 mg/kg

Study 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.

Eligibility

Sex
FEMALE
Min age
3 Years
Max age
15 Years
Healthy volunteers
No
Inclusion Criteria: * Age: Childern between 3:15 years old * American Society of Anesthesiologists(ASA) Physical Status I or II * Elective Tonsillectomy Exclusion Criteria: * Parents refusal * Presence of preoperative sore throat * Known allergy to the study drug * History of upper respiratory tract infection 2 weeks prior to surgery * Mental retardation or inability to communicate * Significant Cardiovascular disease as Heart Block * Post Tonsillectomy bleeding

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Fayoum university Hospitl Al Fayyum Egypt Recruiting

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Other trials for the same condition

Intravenous Regional Analgesia of Dexmedetomidine Enrolling by invitation
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07780760 on ClinicalTrials.gov ↗ ← All trials in Egypt