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

NCT ID: NCT06618547

Last Updated: 2025-06-15

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 140 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-11-30
• Study Completion Date: 2026-11-30

Brief Summary

A Study to Investigate the Effectiveness and Safety of the TENEO 317 Model 2 Excimer Laser to Treat Myopia with or without Astigmatism by Transepithelial Photorefractive Keratectomy

Conditions

Myopia

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

TENEO 317 Model 2 excimer laser

Group Type: EXPERIMENTAL

TENEO 317 Model 2 excimer laser

Intervention Type: DEVICE

TENEO 317 Model 2 excimer laser by Transepithelial Photorefractive Keratectomy

Interventions

TENEO 317 Model 2 excimer laser

TENEO 317 Model 2 excimer laser by Transepithelial Photorefractive Keratectomy

Intervention Type: DEVICE

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.

• Minimum Eligible Age: 22 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Bausch & Lomb Incorporated

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Central Contacts

Dennis Carson

Role: CONTACT

Dennis.Carson@bausch.com

4035025307

Rosangela Nolasco

Role: CONTACT

Rosangela.Nolasco2@bausch.com

9492591633

Other Identifiers

907

Identifier Type: -

Identifier Source: org_study_id