Clinical Trials Directory

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.