MedTrace Logo

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

NCT07175779 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 106

Last updated 2026-03-16

No results posted yet for this study

Summary

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

  • Adenotonsillar Hypertrophy

Interventions

OTHER

Face-to-Face Preanesthesia Consultation

Participants receive a standard preoperative anesthesia consultation in person at the hospital

OTHER

Telemedicine Preanestehsia Consultation

Participants receive a preoperative anesthesia consultation remotely via video conferencing using a secure telemedicine platform.

Sponsors & Collaborators

  • Andrea Saporito

    lead OTHER

Principal Investigators

  • Andrea Saporito, MD, Prof. · Ente Ospedaliero Cantonale, Servizio di Anestesiologia

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Max Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-12-11
Primary Completion
2027-05-31
Completion
2027-05-31

Countries

  • Switzerland

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07175779 on ClinicalTrials.gov