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 @ 5:12 PM
Ignite Modification Date:
2025-12-24 @ 5:12 PM
NCT ID:
NCT02890550
Eligibility Criteria:
Inclusion Criteria for Patients with Alström syndrome:
* Age\> 2 years
* Affiliated with a social security scheme
* Informed consent signed
* Retinal dystrophy and proved at least three diagnostic criteria Alström syndrome (Criteria Marshall et al, 2005):
* Early obesity
* Deafness
* Dilated cardiomyopathy
* Type 2 diabetes
* Hypogonadism
* Absence of polydactyly
* Lack of mental retardation
* A family history of the ALMS
* Mutation in the ALMS gene identified
Inclusion Criteria for Related of Alström patients :
* Father / Mother of a patient diagnosed with Alström
* Age greater than 18 years
* Affiliated with a social security scheme
* Informed consent signed
Exclusion Criteria for Patients with Alström syndrome:
* Current pregnancy (a pregnancy test is routinely performed at baseline)
* Pregnant or breastfeeding women
* Intercurrent diseases do not allow the practice exams in protocol
* Subject to exclusion period (determined by a previous study or a study in progress)
Exclusion Criteria for Related of Alström patients :
* Age less than 18 years
* Subject to exclusion period (determined by a previous study or a study in progress)
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
2 Years
Study:
NCT02890550
Study Brief:
Protocol Section:
NCT02890550