Outcomes of Cataract & Refractive Procedures
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorVision Care Collective Limited
About this trial
The primary objective of the database is to retrospectively analyse the visual and refractive outcomes of cataract and refractive procedures in order to continuously assess outcomes and also compare outcomes between the different IOLs, or the different refractive procedures.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Adult patients who have undergone a refractive procedure
Adult patients who have undergone a cataract procedure with implantation of an intraocular lens
Age ≥ 18 years old
Patient able to consent for their pseudonymised data to be used for research purposes
Disqualifiers
NONE
Trial population
The population for the database will be existing patients of the clinic. These are patients who presented to the clinic with an interest for a refractive or cataract procedure.
Trial design
Design model
Cohort
Time perspective
Retrospective
Treatments tested in this trial
Not listed
Trial groups
150 Participants
are grouped into 1 trial groupGroup A: Patient of the clinic
Trial outcomes
Primary outcomes
1
Post-operative Uncorrected Distance Visual Acuity
Time frame
postoperative visit 3-6 months2
Post-operative Distance Corrected Visual Acuity
Time frame
postoperative visit 3-6 months3
Post-operative subjective refraction (Sphere, Cylinder, Axis)
Time frame
postoperative visit 3-6 months4
Accuracy of post-operative refraction achieved compared to targeted refraction
Time frame
postoperative visit 3-6 monthsSecondary outcomes
1
Comparative analysis - Different types of IOLs
Comparative analysis between different types of IOLs might be performed to investigate whether one IOL might offer additional benefits to patients compared to another IOL.
Time frame
postoperative visit 3-6 months2
Comparative analysis - Refractive procedure
Comparative analysis between different types of refractive procedures might be performed to investigate whether one procedure might offer additional benefits to patients.
Time frame
postoperative visit 3-6 monthsOther outcomes
1
Glare Assessment
For intraocular lens offering a visual benefit at near and/or intermediate, such as multifocal IOLs, EDoF (Extended Depth of Focus) IOLs, enhanced monofocal IOLs, and additional glare perceptions may be assessed.
Time frame
postoperative visit 3-6 monthsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Vision Care Collective Limited
Lead sponsor
Rayner Intraocular Lenses Limited
Collaborator
Source ClinicalTrials.gov