Depression and Anxiety Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- Children up to 16 years of age who are scheduled for a planned tonsil removal or tonsil and adenoid removal surgery.
- Children who fall within a certain range of general health categories as assessed by an anaesthesiologist (classified as ASA I to III — confirm with trial site if unsure what this means).
- Children whose parent or legal guardian is able and willing to give formal written permission for participation.
Who may not be able to join:
- Children whose parent or legal guardian is unable or unwilling to give formal written permission for participation.
- Children whose parent or guardian has declined to take part.
- Children who have medical reasons that make general anaesthesia unsafe for them.
- Children with a known allergy to any of the medicines used as part of the anaesthetic plan for this trial.
- Children whose airway may be difficult to manage during anaesthesia.
- Children with a long-term health condition that is not well controlled, such as asthma.
- Children with a heart condition.
- Children with a genetic disorder.
- Children with a condition affecting their blood, such as a blood disorder, anaemia, or a problem with blood clotting.
- Children with a complex physical disability.
- Cases where the child or their carer has requested not to participate.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Andrea Saporito, MD, Prof., Ente Ospedaliero Cantonale, Servizio di Anestesiologia
Phone: +41918118147
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Incidence of perioperative respiratory adverse events (PRAE); Incidence of PRAE (perioperative respiratory adverse events)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.