Nebulized Dexmedetomidine vs Nebulized Lidocaine for Postoperative Sore Throat in Children

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study compares two nebulized medications given around the time of pediatric tonsillectomy to see which better reduces postoperative sore throat. Children aged 3 to 15 years with ASA I–II undergoing elective tonsillectomy are randomized to receive either dexmedetomidine or lidocaine via nebulization. The goal is to identify a preventive approach that minimizes throat discomfort after surgery without adding safety risks. The trial addresses a common pediatric complication and evaluates patient-friendly delivery with a simple administration method. Outcomes will inform whether nebulized dexmedetomidine offers meaningful relief compared with lidocaine.

Why it matters

Who can join: the full rules

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

Where it's running

• Fayoum university Hospitl
  Al Fayyum, Egypt Recruiting

Study contacts

• Study coordinator: Mustafa Omar Rateb Abdelhafez, MBBCH
• Email: mo114@fayoum.edu.eg
• Phone: 01153599320

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.