Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 4:14 AM
Ignite Modification Date:
2025-12-25 @ 4:14 AM
NCT ID:
NCT03961620
Eligibility Criteria:
Inclusion Criteria:
* ASA score I to IV
* Patients submitted to major surgical procedures at the main OR facilities (or at the ambulatory surgery building for ophthalmologic procedures) under general or neuraxial anesthesia from surgical specialties
* Patients (parents or legal guardians regarding pediatric patients) that have signed informed consent form.
Exclusion Criteria:
* Patients submitted to craniofacial neurosurgical procedures
* Patients submitted to any surgical procedure requiring draping or sterile isolation of the frontal part of head, precluding intraoperative assessment of SpotOn sensor.
* Patients (parents or legal guardians regarding pediatric patients) that have not signed informed consent form.
* Patients that by the time of the hospital admission present a relevant inflammatory or infectious process at the skin of frontal part of the head
* Patients diagnosed with psychiatric disease relevant enough to avoid adequate staff-patients communication for this specific study
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
8 Years
Maximum Age:
100 Years
Study:
NCT03961620
Study Brief:
Protocol Section:
NCT03961620