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:
2025-12-24 @ 7:38 PM
Ignite Modification Date:
2025-12-24 @ 7:38 PM
NCT ID:
NCT07267403
Eligibility Criteria:
Inclusion Criteria:
* Right-handed patient
* Scheduled for surgery using intravenous anesthesia with propofol concentration
Exclusion Criteria:
* Allergy to propofol, soy, or peanuts.
* BMI \< 20 or \> 30
* Pregnant or breastfeeding women
* Medical or surgical history that may interfere with median nerve stimulation or EEG signal acquisition (e.g., diabetes, polyneuropathy, central neurodegenerative disease, epilepsy, brain surgery)
* History of right median nerve injury
* Right upper limb amputation
* Upper limb surgery
* Unable to wear an EEG headset (prone position, head and neck surgery)
* Drug abuse
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
81 Years
Study:
NCT07267403
Study Brief:
Protocol Section:
NCT07267403