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:
2026-03-26 @ 3:15 PM
Ignite Modification Date:
2026-03-26 @ 3:15 PM
NCT ID:
NCT07476768
Eligibility Criteria:
Inclusion Criteria:
* For patients :
* Male or female over 18 years of age with fibrous dysplasia/McCune-Albright syndrome diagnosed by a rheumatologist.
* Mentally and legally able to provide informed consent to participate in the study.
* Affiliated with a health insurance system.
* For healthy volunteers :
* Male or female over 18 years of age.
* Matched to patients by age and sex.
* Mentally and legally able to provide informed consent to participate in the study.
* Affiliated with a health insurance system.
Exclusion Criteria:
* For patients :
* Medical and/or surgical history considered by the investigator or delegated physician to be incompatible with study procedures (e.g., amputation or physical limitation preventing completion of pain assessment tests).
* Recurrent pain at sites planned for stimulation during thermal and mechanical testing (forearms or palms).
* Presence of anxiety and/or depression defined as Hospital Anxiety and Depression Scale (HADS) score \>11.
* Use of analgesic medication within the week preceding inclusion.
* Use of complementary treatments for analgesic purposes (e.g., vitamins, herbal products, cannabinoids).
* Individuals under legal protection (guardianship or trusteeship) or deprived of liberty.
* Pregnant or breastfeeding women.
* Refusal to participate.
* For heathly volunteers :
* Medical and/or surgical history considered by the investigator or delegated physician to be incompatible with study procedures (e.g., amputation or physical limitation preventing completion of pain assessment tests).
* Presence of sleep disorders defined as Pittsburgh Sleep Quality Index (PSQI) score \>5.
* Presence of anxiety and/or depression defined as HADS score \>11.
* Use of analgesic medication within the week preceding inclusion.
* Use of complementary treatments for analgesic purposes (e.g., vitamins, herbal products, cannabinoids).
* Individuals under legal protection (guardianship or trusteeship) or deprived of liberty.
* Pregnant or breastfeeding women.
* Refusal to participate.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07476768
Study Brief:
Protocol Section:
NCT07476768