Effectiveness and Safety of the TENEO 317 Model 2 Excimer Laser to Treat Myopia With or Without Astigmatism by Transepithelial Photorefractive Keratectomy
- Sponsor
- Bausch & Lomb Incorporated
- Study ID
- NCT06618547
- Status
- Not Yet Recruiting
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Conditions
- Myopia
Eligibility Criteria
- Sex
- ALL
- Age
- 22 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- TENEO 317 Model 2 excimer laser — DEVICETENEO 317 Model 2 excimer laser by Transepithelial Photorefractive Keratectomy
Study Details
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
Key Dates
- First listed
- Oct 1, 2024
- Start date
- Nov 30, 2025
- Status verified
- Jun 2025
- Primary completion
- Nov 30, 2026
- Completion
- Nov 30, 2026
Study Design
- Enrollment
- 140 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: TENEO 317 Model 2 excimer laser
Primary Outcome Measure
Maintenance of BCDVA - [ Time Frame: through study completion, an average of 1 year ]
Central Contacts
- Dennis Carson4035025307
- Rosangela Nolasco9492591633
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