About this trial
Prospective, interventional, non-randomized, open-label study, multi-center, Gehan-designed study with sequential inclusions in each subgroup, ranging from 4 subjects to a maximum 37 subjects per subgroup included
Eligibility criteria
Qualifiers
Age ≥ 18 years and < 75 years;
Having received informed information about the study and having signed a consent to participate in the study;
Affiliated or covered by social security
Subjects usually followed at one of the recruiting centers;
Disqualifiers
Persons covered by articles L1121-5 to L1121-8 of the CSP (all protected persons: pregnant women, parturients, nursing mothers, persons deprived of their liberty by judicial decision or administrative decision, minors, and persons under legal protection: guardianship or curatorship);
Women of childbearing age not using an effective method of contraception, or positive pregnancy test (blood or urine);
Participants allergic to tropicamide when using pupillary dilatation;
Inability of the subject to maintain a stable sitting position for research procedures;
Trial design
Treatments tested in this trial
- Images Acquisition