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Clinical Trials in France / NCT07789249
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Quality of Vision After Implantation of EDOF Implants Versus Monofocal Implants in Patients Who Underwent Epiretinal Membrane and Cataract Surgery

NCT07789249 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-09-20
Last updated
2026-08-27

Condition(s) studied

Intraocular ImplantsExtended Depth of Focus

Investigational drug(s) / intervention(s)

QuestionnairesIntermediate visual acuityOptical coherence tomographycataract surgery with intraocular lens implantation

Questionnaires: NEI-VFQ (National Eye Institute Visual Function Questionnaire) 25 before the surgery, 3 months after and 6 months after the surgery.

Intermediate visual acuity: ETDRS (Early Treatment Diabetic Retinopathy Study) scale before the surgery and 1 month, 3 months and 6 months after the surgery

Optical coherence tomography: 1 month, 3 months and 6 months after surgery

cataract surgery with intraocular lens implantation: Two different cataract surgeries : TECNIS monofocal versus PureSee EDOF (extended depth of focus)

Study summary

Phacoexistence, the first surgical procedure performed in France, naturally raises the question of lens replacement. In recent years, the choice of intraocular lenses has expanded considerably. The term EDOF (Extended Depth of Focus) refers to intraocular lenses offering an extended depth of field to improve vision at different distances, while reducing the visual aberrations associated with traditional multifocal lenses.

However, they still generate some optical aberrations that could therefore limit the quality of vision for patients with retinal damage.

With the development and acceleration of cataractogenic processes observed after vitrectomy, the use of combined phaco-vitrectomy surgery has become increasingly common, particularly among patients over 60 years of age. This integrated approach allows for the simultaneous treatment of cataracts and vitreoretinal pathologies, thus reducing the need for subsequent cataract surgery, which frequently develops after vitrectomy. In addition to optimizing the patient care pathway, this technique offers clinical advantages, such as faster visual recovery and fewer complications associated with multiple surgeries. Phacovitrectomy is therefore emerging as a practical and effective solution for managing elderly patients requiring vitreoretinal surgery.

Therefore, in the specific context of macular surgery, often considered less suitable for the use of premium implants, EDOF (Extended Depth of Focus) implants raise some questions. The available data on their performance and tolerability in this specific context remain limited, making their use still poorly defined in these complex clinical situations, except in certain medical macular pathologies.\<sup\>4\</sup\> This study aims to evaluate, within the context of macular surgery, the relevance and potential role of EDOF (Extended Depth of Focus) implants in order to improve the management of these patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Male or female over 18 years of age * Epiretinal membrane with surgical indication * Indication for cataract surgery with intraocular lens implantation * Epiretinal membranes with near visual acuity ≥ P4 * Preserved ellipsoidal zone in the retrofoveal region, without fragmentation or interruption * Central macular thickness less than or equal to 450 microns * Signed informed consent * Patients covered by social security or an equivalent scheme Exclusion Criteria: * Associated ocular pathologies (advanced glaucoma, exudative AMD). * Central macular thickness \> 450 microns * Epiretinal membranes with near visual acuity \< P4 * Previous macular surgery * Contraindication to the implantation of either type of lens * Cognitive impairment, or a disorder causing difficulty understanding instructions or answering questionnaires * Pregnant, parturient, or breastfeeding women, as defined in Article L1121-5 of the French Public Health Code (CSP) * Protected individuals: adults under guardianship, curatorship, or other legal protection, deprived of liberty by judicial or administrative decision. * Patients incapable of personally giving consent, as defined in Article L.1121-8 of the French Public Health Code (CSP), or adults protected by law

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
Clinique du Val d'Ouest - Centre Pôle Vision Aix-en-Provence France
Clinique du Val d'Ouest - Centre Pôle Vision Écully France
Centre Monticelli Paradis Marseille France

More Almaviva Sante trials in France

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07789249 on ClinicalTrials.gov ↗ ← All trials in France