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

Recruiting N/A Interventional Study
Adenotonsillar Hypertrophy
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
Up to 16
Sex
Any
Study type
Interventional
Purpose
Health Services Research
Participants needed
106 (estimated)
Sponsor
Andrea Saporito · Other
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About This Trial
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…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Pediatric patients (up to 16 years of age) undergoing elective tonsillectomy or adenotonsillectomy * ASA (American Society of Anesthesiologists) physical status I to III, * Patients who have a parent or legal guardian able and willing to provide informed consent. Exclusion Cr…
Contacts

Alessandro Genini, MD

+41918118147

alessandro.genini@eoc.ch

CONTACT

Roberto Dossi, MD

+41918119341

roberto.dossi@eoc.ch

CONTACT