Phase
Condition
Panic Disorders
Mood Disorders
Anxiety Disorders
Treatment
Virtual reality immersion
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
All non-ambulatory patients undergoing elective surgery or procedure under generalanaesthesia with intravenous induction
Minimal age of 18 year old
Able to give informed consent for the study as documented by signature
Exclusion
Exclusion Criteria:
Lacking capacity or ability to complete the consent form and/or questionnaire andinterview method and/or incapacity to respond to the required obligations linked tothe study protocol (assessed by the operator)
Known cognitive dysfunction, previous history of neurological/psychiatric diseaselike epilepsy
Depression or anxiety under treatment
Non-Italian speaking patients
Anticipated difficult airway management
Injuries to the head/face that would prohibit wearing headsets
Active nasal bleeding or occlusion, nasal abnormality or recent nasal trauma, recentnasal surgery, significant raised intracranial pressure and base of skull fractures
Any pre-operative premedication, including pharmacological premedication
Rapid sequence induction
Haemodynamic instability
Infectious skin conditions on the head/face
Undrained pneumothorax
Contact isolation due to bacteria and viruses
Symptoms of vertigo or motion sickness
Reduced visual or auditory acuity
BMI > 35 kg/m2
Pregnancy
Claustrophobia
Pre-existing hypoxemia (baseline oxygen saturation < 92% when breathing room air)
Need for an arterial line before general anaesthesia induction
Study Design
Connect with a study center
Istituto Cardiocentro
Lugano, Ticino 6900
SwitzerlandActive - Recruiting
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