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 @ 3:37 AM
Ignite Modification Date:
2025-12-25 @ 3:37 AM
NCT ID:
NCT06347302
Eligibility Criteria:
Inclusion Criteria:
* Subject having given oral, free and informed consent to take part in the study
* Subjects with primary retinal detachment requiring vitrectomy (RD group) Or
* Subject requiring vitrectomy for macular surgery (primary epiretinal membrane or macular hole) (Control group)
Exclusion Criteria:
* Subject not affiliated to or not benefiting from national health insurance
* Pregnant, parturient or breast-feeding women
* Minors
* Subject to a measure of legal protection (curatorship, guardianship)
* Subjects of full age who are incapable or unable to express their consent
* Subject who has already participated in the study
* Subject with recurrent retinal detachment
* Subjects with an epiretinal membrane of secondary origin (OVCR, inflammation, diabetic retinopathy)
* Subject refusing blood sampling
* Subjects with pre-existing retinal pathology (vascular or degenerative retinopathy)
* People with diabetes
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06347302
Study Brief:
Protocol Section:
NCT06347302