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 @ 3:26 AM
Ignite Modification Date:
2025-12-25 @ 3:26 AM
NCT ID:
NCT03914105
Eligibility Criteria:
Inclusion Criteria:
* Healthy subjects aged 18 to 65
* Subjects informed of the constraints of the study and having given their written consent.
* Subjects benefiting from a social security scheme.
Exclusion Criteria:
* Subjects under 18 and over 65
* Subjects who have previously participated in a pain study involving the induced pain test.
* Subjects with serious psychiatric disorders.
* Subjects with a diagnosis of acute or chronic pain.
* Subjects who have been taking antalgic substances for less than a week.
* Subjects with progressive disease not stabilized by medical treatment.
* Women in menstruation.
* Pregnant women.
* Subjects with a score greater than 10 for the Depressive Dimension on Hospital Anxiety and Depression Scale (HADS)
* Subjects with an anxiety score "state" higher than anxiety "traits" on the Spielberger condition state / traits anxiety inventory (STAI)
* Subjects with a score of 32 or higher on the Catastrophe Rating Scale (PCS-CF)
* Non-cooperating person.
* Person under legal protection
* Subjects not benefiting from a social security scheme
* Refusal of participation
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT03914105
Study Brief:
Protocol Section:
NCT03914105