Clinical Investigation of IXIUM TWIN Viscoelastic Ophthalmic Device For Cataract Surgery
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: IXIUM TWIN, HEALON.
- Who it may be relevant to
- Registry conditions: Cataract Surgery. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Randomized Clinical Investigation Of The IXIUM TWIN Viscoelastic Ophthalmic Device (OVD) For Cataract Surgery With Intraocular Lens Implantation
Overview
This clinical trial is testing a new surgical gel called IXIUM TWIN, designed to protect the eye during cataract surgery. Cataracts, which cloud the eye's natural lens, are the leading cause of vision loss worldwide. Surgery to remove the cataract and replace it with an artificial lens is the standard treatment, and viscoelastic gels like IXIUM TWIN are used to keep the eye stable and safe during the procedure. The goal of this study is to compare IXIUM TWIN with an already approved gel (HEALON) to ensure it works just as well (or better) in protecting the delicate cells inside the eye. Specifically, researchers will measure whether IXIUM TWIN causes less damage to the eye's inner lining (endothelial cells) after surgery. Who can take part? Adults aged 18 and older who have cataracts and are scheduled for surgery may qualify. Only one eye per participant will be included. Patients must be able to attend follow-up visits and provide informed consent. What does participation involve? Before surgery, participants will have eye exams to check vision, cell health, corneal thickness, and eye pressure. During surgery, they will randomly receive either IXIUM TWIN or HEALON (neither the patient nor the surgeon will choose). After surgery, follow-up visits at 1 day, 7 days, 30 days, and 90 days will monitor healing, vision improvement, and any side effects. Potential risks and benefits As with any cataract surgery, there are minor risks, such as temporary increased eye pressure, inflammation, or swelling, but these are rare and usually resolve quickly. The benefits include improved vision after cataract removal. If successful, IXIUM TWIN could offer surgeons another high-quality option for protecting the eye during surgery. Study timeline Patient enrollment begins in January 2025 and ends in June 2025, with follow-ups completing by September 2025. The full study is expected to conclude in early 2026. This study is sponsored by LCA Pharmaceutical and will take place at four hospitals in France. Participation is voluntary, and patients can withdraw at any time.
Interventions
- Device IXIUM TWIN
Use of IXIUM TWIN as the Ophthalmic Viscosurgical Devices in the cataract surgery - Device HEALON
Use of HEALON as the Ophthalmic Viscosurgical Devices in the cataract surgery
Primary outcome measures
- Percentage of Endothelial Cell Loss between pre- and post-operative periods [Time frame: 90 days]
Secondary outcome measures (7)
- Proportion of patients with intraocular pressure (IOP) ≥30 mmHg [Time frame: 90 days]
- Slit-lamp biomicroscopy [Time frame: 90 days]
- Pachymetry [Time frame: 90 days]
- Best-corrected visual acuity (BCVA) for distance and near vision [Time frame: 90 days]
- Assessment of the viscoelastic device (DM) behavior [Time frame: Post-op]
- Patient satisfaction assessment regarding the procedure (Likert scale) [Time frame: 90 days]
- Assessment of adverse events [Time frame: 90 days]
Eligibility criteria
Inclusion criteria
- Adult patients (≥18 years) with cataract (described and coded per WHO classification²⁷)
- One eye per patient enrolled in the clinical investigation (IC)
- Intraocular pressure (IOP) controlled or uncontrolled with treatment
- Cataract extraction via phacoemulsification with implantation of a posterior chamber injectable intraocular lens (IOL) through a small incision
- Signed informed consent from both patient and physician
- Patient capable of understanding the IC procedures and geographically stable
- Patient covered by or eligible for a social security/health insurance system
Exclusion criteria
- Patient unable to participate in a clinical investigation (IC)
- Pregnant women or those at risk of pregnancy during the study
- Patient under legal guardianship (tutelle), conservatorship (curatelle), or judicial protection (sauvegarde de justice)
- Patient currently enrolled in another clinical investigation at the time of inclusion
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Double blind
- Primary purpose
- Supportive care
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07279506 · 2024-A01718-39 · 2024-A01718-39