Actively Recruiting

Phase Not Applicable
Age: 0 - 16Years
All Genders
NCT07175779

Teleconsultation vs Face-to-Face Evaluation for Perioperative Respiratory Events in Pediatric Adenotonsillectomy

Led by Andrea Saporito · Updated on 2026-03-16

106

Participants Needed

1

Research Sites

72 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this clinical trial is to assess whether preoperative anesthesia teleconsultation is at least equivalent to in-person consultation in preventing perioperative respiratory adverse events (such temporary reduction in oxygen levels in the blood) in the operating room and in the first 24 hours after the surgery in pediatric adenotonsillectomy. Researchers will compare the teleconsultation to in-person consultation to see if there is a difference in the frequency of respiratory adverse events in the operating room and during the first 24 hours after adenotonsillectomy. Participants will: \- undergo a traditional in-person anesthesiology consultation scheduled at the hospital or a online preoperative anesthesiology teleconsultation.

CONDITIONS

Official Title

Teleconsultation vs Face-to-Face Evaluation for Perioperative Respiratory Events in Pediatric Adenotonsillectomy

Who Can Participate

Age: 0 - 16Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Pediatric patients up to 16 years old undergoing elective tonsillectomy or adenotonsillectomy
  • ASA (American Society of Anesthesiologists) physical status I to III
  • Parent or legal guardian able and willing to provide informed consent
Not Eligible

You will not qualify if you...

  • Parent or guardian unable or unwilling to provide informed consent
  • Refusal to participate by parent or guardian
  • Patients with contraindications to general anesthesia
  • Known allergy to any drugs used in the anesthetic protocol
  • Potential difficult airway
  • Poorly controlled chronic illness such as asthma
  • Cardiac disease
  • Genetic disorder
  • Hemoglobinopathy, anemia, or clotting problems
  • Complex physical disability
  • Request from the patient or carer

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Ospedale Regionale Bellinzona e Valli

Bellinzona, Canton Ticino, Switzerland, 6500

Actively Recruiting

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Research Team

A

Alessandro Genini, MD

CONTACT

R

Roberto Dossi, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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