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:
2025-12-26 @ 1:18 PM
Ignite Modification Date:
2025-12-26 @ 1:18 PM
NCT ID:
NCT06014606
Eligibility Criteria:
Inclusion Criteria:
* Willingness to sign an informed consent
* Age between 18 and 35
* Body-Mass Index (BMI) between 17.5-30
* Availability for participation through the duration of the study
Exclusion Criteria:
* Diagnosis of a psychiatric or neurological disorder, including substance abuse or dependence (yes/no self-report - lifetime)
* Use of any psychopharmacological treatment 3 weeks before the test day (yes/no self-report)
* Use of any blood pressure medication (yes/no self-report - lifetime)
* Pregnancy (confirmed via urine pregnancy test) or nursing (yes/no self-report) or have plans to get pregnant in the near future (yes/no self-report) (females only)
* Diagnosis of a cardiac disease (medical questionnaire), obstructive respiratory disease (medical questionnaire), abnormal blood pressure (diastolic\< 60mmHg; systolic\< 90mmHg) (medical screening)
* Chronic renal failure (medical questionnaire)
* Hypothyroidism (medical questionnaire)
* Diabetes (medical questionnaire)
* Hypersensitivity to phenothiazines (medical questionnaire)
* Diagnosis of a cardiac disease (medical questionnaire)
* Alcohol consumption in the 24 hours before the test session starts (yes/no self-report)
* Food intake less than 3 hours before the test day (yes/no self-report)
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT06014606
Study Brief:
Protocol Section:
NCT06014606