Effectiveness and Safety of the TENEO 317 Model 2 Excimer Laser to Treat Myopia With or Without Astigmatism by Transepithelial Photorefractive Keratectomy

Launched by BAUSCH & LOMB INCORPORATED · Sep 26, 2024

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ClinConnect Summary

This clinical trial is studying a new laser treatment called the TENEO 317 Model 2 Excimer Laser to help people with myopia (nearsightedness) and possibly astigmatism. The goal is to see how effective and safe this treatment is when performed using a technique called transepithelial photorefractive keratectomy (PRK). Participants in the trial must be at least 22 years old and have good corrected vision (20/25 or better) in the eye being treated. They should also have a stable vision prescription for at least a year and meet other specific health criteria.

For those who qualify, the trial will involve stopping the use of contact lenses for a short period before the procedure and attending follow-up visits after the treatment to monitor their recovery. It's important to note that some individuals, such as those with certain eye conditions or illnesses that could complicate surgery, may not be eligible. Overall, this study aims to provide more options for those struggling with myopia and to ensure the safety and effectiveness of this new treatment approach.

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Eligibility criteria

• Inclusion Criteria:
• • 1. 22 years of age or older at the time of the pre-operative examination.
• • 2. Best distance corrected visual acuity (BCDVA) 20/25 or better in the study eye
• • 3. Difference between manifest refractive spherical equivalent (MRSE) and the cycloplegic refraction of ≤ 0.75 D in the study eye.
• • 4. Stable refraction (i.e., a change of ≤ 0.50 D in MRSE) for a minimum of 12 months before surgery, as verified by consecutive refractions, medical records, or prescription history.
• • 5. Agree to discontinue contact lenses for at least two weeks (for rigid or toric lenses) or three days (for soft contact lenses) before the first refraction to establish stability and through the day of surgery.
• • 6. A stable refraction (within ± 0.50 D) after discontinuation of contact lens(es), as determined by MRSE between two consecutive examinations at least one week apart.
• • 7. Normal corneal topography per the investigator in the study eye.
• • 8. Anticipated postoperative stromal thickness of at least 350 microns.
• • 9. Ability to lie flat without difficulty.
• • 10. Willing and able to read, understand, and sign a written informed consent form (ICF)
• • 11. Willing and able to comply with the schedule for all post-surgery follow-up visits.
• • 12. Pre-operative myopic refractive error with sphere component from -0.25 D to -8.00 D in each operative eye, with or without cylinder from 0.00 D to -3.00 D, based on the manifest refraction with treated MRSE of -0.25 D to -9.50 D.
• Exclusion Criteria:
• • 1. Acute or chronic disease or illness that would increase operative risk or confound the results of the study (e.g., dry eye, cataract, immuno-compromise, rheumatoid arthritis, clinically significant atopic disease, acne rosacea, autoimmune disease, endocrine disorders, lupus, systemic connective tissue disease, diabetes, or severe atopic disease).
• • 2. Use of medications that may increase risk to the subject or may confound the outcome of the study, including those known to affect wound healing (e.g., systemic corticosteroids, antimetabolites)
• 3. Ocular conditions that may predispose the subject to future complications, including but not limited to:
• • 1. Evidence or history of retinal vascular disease
• • 2. History or evidence of active corneal disease or infection (e.g., recurrent corneal erosion syndrome, herpes simplex or herpes zoster keratitis) in either eye.
• • 3. History of or evidence of glaucoma or glaucoma suspect (e.g., IOP \> 21 mmHg).
• • 4. Previous intraocular or corneal surgery in an eye considered for eligibility that might confound the study's outcome or increase the subject's risk.
• • 5. An increased risk for developing strabismus post-treatment or an ocular muscle disorder (e.g., strabismus or nystagmus) affecting fixation.
• • 6. Known sensitivity to any study medications (e.g., used during TransEpi PRK procedure and postoperative care).
• • 7. Central corneal scars affecting visual acuity.
• • 8. Presence of keratoconus, subclinical or forme fruste keratoconus, corneal dystrophy, or other corneal irregularity (e.g., irregular astigmatism).
• • 9. Presence of visually significant or progressive cataract in an eye considered for eligibility.
• • 10. Actively taking medications contraindicated with TransEpi PRK, such as isotretinoin (Accutane®) or amiodarone hydrochloride (Cordarone®).
• • 11. Cardiac pacemaker, implanted defibrillator, or another implanted electronic device.
• • 12. Pregnant, lactating, or subjects who plan to become pregnant during the study.
• • 13. Participation in any other clinical trial within 30 days of screening or during this clinical trial.14. Subjects for whom the pre-operative assessment of the cornea/ eyes indicates that one or both eyes are not suitable candidates for treatment based upon the investigator's medical judgment.
• • 15. Treated eye with mesopic pupil size \> 7.0 mm.