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Compares treatment options for Adenotonsillar Hypertrophy
Official title Teleconsultation vs Face-to-Face Evaluation for Perioperative Respiratory Events in Pediatric Adenotonsillectomy
ClinicalTrials.gov ID: NCT07175779
What this study is testing
- What it's testing
- 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.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages up to 16
You may be able to join if
- 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.
You likely can't join if
- Parent or guardian unable or unwilling to provide informed consent,
- Refusal to participate by parent/guardian,
- Patients with contraindications to general anesthesia,
- Known allergy to any drugs used in the anesthetic protocol.
- Potential difficult airway,
- Poorly controlled chronic illness (e.g. asthma),
See the full eligibility 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.
- Parent or guardian unable or unwilling to provide informed consent,
- Refusal to participate by parent/guardian,
- Patients with contraindications to general anesthesia,
- Known allergy to any drugs used in the anesthetic protocol.
- Potential difficult airway,
- Poorly controlled chronic illness (e.g. asthma),
- Cardiac disease ,
- Genetic disorder,
- Haemoglobinopathy, anemia or clotting problem,
- Complex physical disability,
- Request from the patient or carer
The study team makes the final eligibility decision.
Where it's taking place
- Bellinzona, Canton Ticino, Switzerland
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, up to 16 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Bellinzona, Canton Ticino, Switzerland. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.