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 @ 9:38 PM
Ignite Modification Date:
2025-12-24 @ 9:38 PM
NCT ID:
NCT04205032
Eligibility Criteria:
Inclusion Criteria:
* Height between 160 et 180 cm
* Body mass index between 18 et 24
* Normal blood pressure, heart rate and cardio-pulmonary auscultation at rest
* Normal electrocardiogram
* Possibility to perform transcranial doppler
* Able to understand aims and constraints of this study
* National health insurance
* Signature of the informed consent form
Exclusion Criteria:
* Pregnant woman (Beta HCG - human chorionic gonadotropin - with urinary test) or breastfeeding
* Participating at the time to another clinical trial investigating
* Reached or surpassed the annual amount of financial compensation allowed by clinical trials (according to French regulation)
* Taking any chronic treatment
* Any sign of cardiovascular or respiration disease
* Any sign of syncopal events by questioning (\>2 events per year)
* Contraindication to perform physical activity
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT04205032
Study Brief:
Protocol Section:
NCT04205032