Last updated: December 5, 2022
Sponsor: Vienna Institute for Research in Ocular Surgery
Overall Status: Active - Enrolling
Phase
N/A
Condition
Eye Disorders/infections
Vision Loss
Eye Disease
Treatment
N/AClinical Study ID
NCT05639075
Voptica
Ages 21-105 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Pseudophakic patients with an Art 40 IOL in one eye and the standard monofocal ICB00IOL in the other eye. A larger series of patients was operated in this way at Hanuschhospital in 2021 and 2022 as the department has the strategy of implanting a new IOLthat has come to market in only one eye and the standard monofocal IOL in thecontralateral eye to reduce potential risks, even though the new IOL had a CE mark andwas readily available on the market.
- Surgery should have been at least 1 month prior to study recruitment
- Age 21 or older
- Visual acuity > 0,8
- Normal findings in the medical history and physical examination unless theinvestigator considers an abnormality to be clinically irrelevant
- Able to walk without walking aids
- Written informed consent prior to commencing study measurements.
Exclusion
Exclusion Criteria:
- nystagmus or pathologies that might affect patient's fixation or physical handicapsthat may decrease gait stability
- any ophthalmic comorbidity that may compromise the visual function or might interferewith the experiments (e.g., macular degeneration, corneal scars, pupil abnormalities,glaucoma)
- reduced contrast sensitivity, binocularity, and stereoscopic vision (e.g., amblyopia,strabismus)
- limitation of age-equivalent gait performance because of neurological,cardio-respiratory or musculoskeletal functional deficits
- pregnancy (pregnancy test will be performed in women of reproductive age)
Study Design
Total Participants: 12
Study Start date:
November 01, 2022
Estimated Completion Date:
November 01, 2024
Study Description
Connect with a study center
Vienna Institute for Research in Ocular Surgery
Vienna, 1140
AustriaSite Not Available
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