A Prospective, Randomized Clinical Study of Two Phakic Toric Implantable Lenses

NCT06839898 | Recruiting DMC

• 2 other identifiers: BTVCPL-PHAKICTORIC-2019-13CIV- 20-09-034764
• Study Type: interventional
• Target: 172
• Locations: 2 countries
• Sites: 4

Brief Summary

Primary Objective: To compare the efficacy and the residual refractive error of EYECRYLTM Phakic toric versus Visian® Toric ICL in moderate to high myopic patient with co-existing astigmatism. Secondary Objectives: To evaluate and compare the safety of EYECRYLTM Phakic toric versus Visian® Toric ICL in moderate to high myopic patients with co-existing astigmatism.

Conditions

Myopia, Moderate; Myopic Astigmatism; Myopia, Degenerative

Outcome Measures

Primary Outcomes (1)

• The mean residual refractive error

  The mean residual refractive error in the study lens population that is equivalent to the mean residual refractive error of the control lens within +/- 0.50 Diopters at the 6-months post-op visit.

  6 Month

Study Arms (2)

EYECRYLTM Phakic Toric Intraocular Lens Treatment Arm

EXPERIMENTAL

Patients will be implanted with Eyecryl Phakic Toric IOL based on randomization.

Device: EYECRYLTM Phakic Toric Intraocular Lens Treatment Arm

Visian® Toric ICL Treatment Arm

ACTIVE COMPARATOR

Patients will be implanted with Visian® Toric ICL based on randomization.

Device: Visian® Toric ICL Treatment Arm

Interventions

EYECRYLTM Phakic Toric Intraocular Lens Treatment Arm DEVICE

The patients will be implanted with Eyecryl Phakic IOL at this arm based on randomization.Phakic intraocular lenses are clear implantable lenses that are surgically placed either in anterior chamber (AC) or posterior chamber (PC) without removing the natural lens, enabling light to focus on the retina for improved uncorrected visual acuity. Phakic intraocular lenses demonstrate high optical quality and potential gain in visual acuity in myopic patients due to retinal magnification. Toric version of phakic intraocular lens is intended to correct both myopia and astigmatism.

EYECRYLTM Phakic Toric Intraocular Lens Treatment Arm

Visian® Toric ICL Treatment Arm DEVICE

The patients will be implanted with Visian® Toric Implantable Contact Lens at this arm based on randomization. Phakic intraocular lenses are clear implantable lenses that are surgically placed either in anterior chamber (AC) or posterior chamber (PC) without removing the natural lens, enabling light to focus on the retina for improved uncorrected visual acuity. Phakic intraocular lenses demonstrate high optical quality and potential gain in visual acuity in myopic patients due to retinal magnification. Toric version of phakic intraocular lens is intended to correct both myopia and astigmatism.

Visian® Toric ICL Treatment Arm

Eligibility Criteria

• Age: 21 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patients 21 years old or older.
• Calculated IOL Power is within the range of the investigational IOLs
• Corneal Cylindrical error within the range defined in the clinical investigation plan
• Subject has monocular UCVA 0.5 LogMAR or worse
• Subject has had a stable refraction (±0.5D; ±1.0D for higher refractive errors), as expressed by manifest refraction spherical equivalent (MRSE) for a minimum 12 months prior to surgery, verified by consecutive refractions and/or medical records or prescription history.
• Subject, who is a current contact lens wearer, needs to demonstrate a stable refraction (±0.5D) expressed as MRSE, on two consecutive examination dates and stability of the refraction is determined by the following criteria:
• Contact lenses were not worn for at least 2 weeks or 3 days prior to the first refraction.
• Two refractions were performed at least 7 days apart.
• Subject, who is expected to have residual postoperative cylindrical refractive error of ≥1D, has been given the opportunity to experience his/her best spectacle vision with the anticipated correction.
• Expected dilated pupil size at least large enough to visualize the axis marking.
• Patients willing to attend all follow-up appointments
• Patients must sign and be given a copy of the written Informed Consent form

You may not qualify if:

• Subject with acute and chronic disease or illness that would increase the operative risk or confound the outcomes of the evaluation.
• Subject taking systematic medication that can confound the outcome of the study or increase the risk to the subject
• Subject with ocular condition that may predispose the subject to future complications
• Subject with previous intraocular or corneal surgery
• Subject with less than the minimum endothelial cell density 2000 cells/mm² at the time of enrollment
• Pregnant or planning to become pregnant, or is lactating during the course of the evaluation
• Other condition associated with fluctuation of hormones
• ACD measured from the endothelium lower than 2.8 mm
• Concurrent participation in another drug or device evaluation.
• Any cataract of any grade.
• Coefficient of variation of endothelial cell area \>0.45
• Percent Hexagonality of endothelial cell shape ≤ 45%
• Monocular subject
• Vulnerable subjects as defined in section 12.3.10

Sponsors & Collaborators

• Biotech Healthcare Holding Gmbh: lead

Study Sites (4)

Precise Vision Augentagesklinik Greven

Münster, North Rhine-Westphalia, 48268, Germany

RECRUITING

Precise Vision Augentagesklinik Rheine

Rheine, North Rhine-Westphalia, 48429, Germany

RECRUITING

Precise Vision Augentagesklinik Rheine

Steinfurt, North Rhine-Westphalia, 48429, Germany

RECRUITING

Netradhama Superspeciality Eye Hospital

Bangalore, Karnataka, 560 082, India

RECRUITING

MeSH Terms

Conditions

Myopia; Lymphoma, Follicular; Astigmatism; Myopia, Degenerative

Condition Hierarchy (Ancestors)

Refractive Errors; Eye Diseases; Lymphoma, Non-Hodgkin; Lymphoma; Neoplasms by Histologic Type; Neoplasms; Lymphoproliferative Disorders; Lymphatic Diseases; Hemic and Lymphatic Diseases; Immunoproliferative Disorders; Immune System Diseases

Central Study Contacts

BHARGAV D JOSHI, M.Sc.

CONTACT

917966823000; bhargav.joshi@biotechhealthcare.com

Hatice B Deveci Summer, B.Sc

CONTACT

0491739106424; basak.deveci@biotechhealthcare.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Model Details: Phakic intraocular lenses are clear implantable lenses that are surgically placed either in anterior chamber (AC) or posterior chamber (PC) without removing the natural lens, enabling light to focus on the retina for improved uncorrected visual acuity. Phakic intraocular lenses demonstrate high optical quality and potential gain in visual acuity in myopic patients due to retinal magnification. Toric version of phakic intraocular lens is intended to correct both myopia and astigmatism

Study Record Dates

• First Submitted: January 9, 2025
• First Posted: February 21, 2025
• Study Start: October 10, 2021
• Primary Completion: August 1, 2025
• Study Completion (Estimated): February 1, 2027
• Last Updated: February 21, 2025

Record last verified: 2025-02

Data Sharing

• IPD Sharing: Will not share

Locations

IN (1); DE (3)