Comparative Study of 3 Multifocal Intraocular Lenses in Murcia

Last updated: March 15, 2024
Sponsor: Cristalens Industrie
Overall Status: Active - Recruiting

Phase

N/A

Condition

Vision Loss

Eye Disorders/infections

Eye Disease

Treatment

intraocular lens implantation in cataract surgery

Clinical Study ID

NCT06323915
2020_03_C3M
  • Ages 50-85
  • All Genders

Study Summary

The goal of this clinical trial is to compare the performance of 3 intraocular lenses (IOLs): FineVision (comparator), ARTIS SYMBIOSE (study lenses), and Tecnis Synergy (comparator) through binocular distance-corrected defocus curve.

This main objective will be to show superiority of the ARTIS SYMBIOSE system through binocular distance-corrected defocus curve.

The patient population to be included is patient suffering from cataract who requires cataract surgery procedure that meet the inclusion and non-inclusion criteria and provide written informed consent.

Participants will attend a total of 5 study visits: 1 preoperative visit, 1 surgery visit and 3 postoperative visits.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • 50 < Age < 85 years old
  • Bilateral age-related cataract
  • Signed informed consent of the study
  • Availability, willingness and sufficient cognitive awareness to comply withexamination procedures
  • Qualify for bilateral implantation within 1 month
  • No previous refractive or ocular surgery
  • Need for IOL in this diopter range: 10 to 30 D
  • Expected postoperative astigmatism ≤ 0.75 D
  • Eye dryness ≤ 2 in dry eye severity grading Non-inclusion criteria:
  • Being under guardianship / curatorship
  • Illiterate or not enough knowledge of Spanish language
  • Acute or chronic disease or illness that would increase risk or confound study resultsfound to be relevant by the investigators
  • Pupil > 4mm or < 2mm in photopic conditions
  • Occupation requiring night-time driving or any occupation incompatible withmultifocality
  • Amblyopia, strabismus, color blindness
  • Extremely shallow anterior chamber
  • Capsule or zonular abnormalities that may affect postoperative centration or tilt ofthe lens (e.g. pseudoexfoliation syndrome, uveitis, Marfan's syndrome).
  • Pupil abnormalities (non-reactive, tonic pupils, abnormally shaped pupils or pupilsthat do not dilate under mesopic/scotopic conditions).
  • Irregular astigmatism, unstable cornea.

Exclusion

Exclusion Criteria:

  • Inability to place the intraocular lens safely at the location planned
  • Surgical complications (e.g. non-circular rhexis, oversized or undersized rhexis).Each patient with these intraoperative complications should not be implanted with thestudy IOL

Study Design

Total Participants: 84
Treatment Group(s): 1
Primary Treatment: intraocular lens implantation in cataract surgery
Phase:
Study Start date:
April 20, 2021
Estimated Completion Date:
September 20, 2025

Study Description

This trial is a single center, prospective, randomized (1:1), unblinded, controlled study conducted in Spain according to Art. 82 MDR (PMCF study).

The lead investigator at the Murcia Clínica Vista Ircovisión (Murcia Ircovision Eye Clinic) is Dr. Jerónimo LAJARA BLESA.

This study examines the visual performance of the three IOLs involved : ARTIS Symbiose (study lens) compared to FineVision (comparator), and Tecnis Synergy (comparator) in bilaterally implanted patients.

Due to the design of the ARTIS SYMBIOSE set of multifocal IOLs and the Tecnis Synergy multifocal IOL that target continuous sharp vision from far vision to near vision, this comparative trial is needed to evaluate if these approaches are able to achieve the enhancement in the patients' depth-of-field that has been reported with the FineVision trifocal IOL, which is considered as the "gold standard".

A total of approximately 84 patients will be included at 1 clinical center. Subjects participating in the study will attend a maximum of 5 study visits (1 preoperative, 1 operative and 3 postoperative visits) over a period of 12 months.

Only patients who have age-related cataracts will be included in the study. To participate in this study, patients must be at least 50 years old at the time of screening and maximum 85 years old. All patients who would like to take part in this study will receive a detailed study information by the investigator staff and a written informed form. Before a patient is admitted, he or she must sign a consent form.

The primary study endpoint is to compare the performance of 3 IOLs (FineVision, ARTIS SYMBIOSE, and Tecnis Synergy) through binocular distance-corrected defocus curve.

The entire study including data processing will be carried out in accordance with EN ISO 14155:2020 Clinical Investigation of Medical Devices for Human Subjects, EN ISO 11979-7:2018: Clinical investigations of intraocular lenses for the correction of aphakia, EU MDR 2017/745, MEDDEV 2.7.1 rev. 4 Clinical Evaluation: A Guide for Manufacturers and Notified Bodies, MPDG:2020: Medical Device Law Implementation Act, as well as applicable local regulations and the Declaration of Helsinki.

Connect with a study center

  • Vista Clinic Ircovision Murcia

    Murcia, 30008
    Spain

    Active - Recruiting

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