Clinical Trial With PRECIZON Presbyopic
Study Details
Study Description
Brief Summary
The purpose of this clinical trial is to evaluate the effectiveness of the PRECIZON Presbyopic.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Prospective, open-label, single-arm, multicenter clinical evaluation with a 3 months follow-up. The PRECIZON Presbyopic is a lens intended for implantation in the capsular bag, indicated for optical correction of aphakia in adults whom the crystalline lens has been removed and who desire presbyopia correction. The main objective is to evaluate the ability of the PRECIZON Presbyopic to provide near, intermediate and distance vision in patients undergoing cataract extraction / Clear Lens Exchange (CLE) and intraocular lens implantation. Study results will be used for CE-approval and registration and marketing purposes.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Intervention arm Bilateral implantation with PRECIZON Presbyopic intraocular lens |
Device: PRECIZON Presbyopic
Optical correction of aphakia in adults in whom the crystalline lens has been removed and who desire presbyopia correction.
Other Names:
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Outcome Measures
Primary Outcome Measures
- Improvement in monocular and binocular uncorrected and corrected near visual acuity [3 months follow-up postoperative]
The ability of the PRECIZON Presbyopia Intraocular lens (IOL) to provide near visual acuity
- Improvement in monocular and binocular uncorrected and corrected intermediate visual acuity [3 months post-op]
The ability of the PRECIZON Presbyopia Intraocular lens (IOL) to provide intermediate visual acuity
- Improvement in monocular and binocular uncorrected and corrected distance visual acuity [3 months post-op]
The ability of the PRECIZON Presbyopia Intraocular lens (IOL) to provide distance visual acuity
Secondary Outcome Measures
- Photopic contrast sensitivity as measured by a contrast sensitivity chart [3 months postoperative]
Binocular contrast sensitivity scores for spatial frequencies of 3.0 cpd, 6.0 cpd, 12.0 cpd and 18.0 cpd.
- Mesopic contrast sensitivity as measured by a contrast sensitivity chart [3 months post-op]
Binocular contrast sensitivity scores for spatial frequencies of 3.0 cpd, 6.0 cpd, 12.0 cpd and 18.0 cpd.
- Stability of manifest refraction (MRSE) as measured by a mean change in MRSE between visits as determined by a paired analysis [3 months post-op]
Percentage of eyes that achieve a change of less than or equal to 1.00 D of MRSE between two refractions performed 3 months apart
- Spectacle dependency [3 months post-op]
Percentage of patients that achieve complete spectacle independence or occasional use of glasses for near or intermediate vision
- Defocus curve [3 months post-op]
Binocular defocus evaluation will be obtained by using the best corrected distance refraction and then defocusing the image in 0.5 D increments to -0.5 D.
- Rates of adverse events and complications [3 months post-op]
- Patient satisfaction as measured by a patient satisfaction questionnaire [3 months post-op]
- Quality of vision as measured by the Quality of Vision (QoV) questionnaire [3 months post-op]
Percentage of patients with a QoV score >10 and >30 at 3 months postoperative
Eligibility Criteria
Criteria
Inclusion Criteria:
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Presbyopic
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Cataract patient or Clear Lens Extraction (CLE) candidate
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Patients wishes to be spectacle independent for near and far vision
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Patient lifestyle and outlook fit with multifocal IOL implantation
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Qualifies for bilateral implantation
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Patient must have a calculated IOL power within the available diopter range
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Expected best corrected visual acuity of 0.5 Snellen decimal or better after IOL implantation.
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No secondary surgical procedure planned during the course of the study
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Availability, willingness and sufficient cognitive awareness and physical ability to comply with examination procedures throughout the entire duration of the study
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Patients must provide written informed consent
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The predicted keratometric postoperative astigmatism (calculated with respect to the surgical induced astigmatism) must be <1.0 D.
Exclusion Criteria:
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Ocular disease other than cataract that may predispose for future complications or might confound the outcome of the investigation (e.g. anterior segment pathology, glaucoma, corneal dystrophy, ocular inflammation, pseudoexfoliation syndrome, retinal disorders)
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Acute or chronic disease or illness or use of medication that could confound the outcome of the study or increase the risk to the subject
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Endothelial cell count <1500 cells/mm2
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Amblyopia
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Congenital eye abnormalities
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Previous ocular surgery that might confound the outcome of the investigation or increase risk to patient
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Concurrent participation or participation during the last 30 days in any other clinical trial
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Patient must not be pregnant or has another condition with associated fluctuation of hormones that could lead to refractive changes
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Medipolis | Wilrijk | Belgium | 2610 | |
| 2 | Universitäts-Augenklinik Heidelberg | Heidelberg | Germany | 69120 | |
| 3 | Academisch Ziekenhuis Maastricht | Maastricht | Limburg | Netherlands | 6229 HX |
| 4 | Oftalvist CIO Jerez | Jerez de la Frontera | Spain | 11408 | |
| 5 | Hospital Universitari Mútua Terrassa | Terrassa | Spain | 08221 | |
| 6 | Acibadem Maslak Hospital | Istanbul | Turkey | 34457 |
Sponsors and Collaborators
- Ophtec BV
Investigators
- Principal Investigator: Mike P. Holzer, Prof. Dr., Heidelberg University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- AP01000538