Trials / Terminated
TerminatedNCT04796662
CT Lucia 601 IOL Implantation in the Sulcus
- Status
- Terminated
- Phase
- —
- Study type
- Observational
- Enrollment
- 62 (actual)
- Sponsor
- Universitaire Ziekenhuizen KU Leuven · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
To perform a retrospective investigation of the CT Lucia 601 IOL implantation in the sulcus
Detailed description
The purpose of the study is to collect data that are parameters of post-IOL implantation safety: * Questionnaire on subjective quality of vision * Centration and anteroposterior position of the IOL (using biometry) * Presence and quantification of any inflammation or pigment present in the anterior chamber (flare meter) * Refractive outcome, with calculation of customized A-constant of the CT Lucia 601 IOL in-the-sulcus and quantification of higher-order aberrations (HOA) * General safety-parameters: * Visual acuity * Intra-ocular pressure * Presence of macular edema or retinal nerve fiber layer (RNFL) thinning (SD-OCT) * Any adverse ophthalmic events
Conditions
Timeline
- Start date
- 2021-03-08
- Primary completion
- 2023-02-20
- Completion
- 2023-02-20
- First posted
- 2021-03-15
- Last updated
- 2023-02-24
Locations
1 site across 1 country: Belgium
Source: ClinicalTrials.gov record NCT04796662. Inclusion in this directory is not an endorsement.