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 @ 9:08 PM
Ignite Modification Date:
2025-12-24 @ 9:08 PM
NCT ID:
NCT02812004
Eligibility Criteria:
Inclusion Criteria:
* the subject's written consent to participate in the present study
* considerable impairment of quality of life (defined as utility value score ≤ 0.7) due to floater-related symptoms for at least 3 months prior to inclusion
* floaters must be located at a safe distance to both the retina and the intraocular lens - preferably in the middle third of the vitreous
* pseudophakic eyes
* age \>18 years
Exclusion Criteria:
* phakic eyes
* any retinal pathology and/or other ocular condition (including but not limited to amblyopia, pathologies of the cornea, glaucoma/history of elevated intraocular pressure) that may prevent or reduce a potential increase in visual acuity and/or decrease of the utility value score and/or incur an increased likelihood of adverse events.
* any ocular or systemic condition that may result in an impaired feasibility of the study treatment and/or required examinations.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
105 Years
Study:
NCT02812004
Study Brief:
Protocol Section:
NCT02812004