Comparing three methods for correcting myopia
Official title: Comparative Study of SMILE, ICL, and Wavelight Plus Alcon Technologies in Myopia Correction
Run by Beijing Visionly Plus Eye Hospital · NCT06788418 · Data updated 2026-11-12
This study tests three different ways to correct nearsightedness to see which one works best and makes patients the happiest.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 40 Years |
| Sex | All |
| Enrollment | 1000 (estimated) |
| Sponsor | Beijing Visionly Plus Eye Hospital Academic / other |
| Locations | 2 sites (Beijing and 1 other locations) |
| Status | Recruiting |
| Started | January 20, 2025 |
| Main results expected | December 31, 2025 |
| Study ends | December 31, 2025 |
| Registry record updated | January 23, 2025 |
| Trial ID | NCT06788418 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults aged 18-40 with a spherical equivalent of -1.00 to -10.00 D and stable refraction for at least 12 months.
✕Probably not a fit
Patients with other ocular pathologies, previous refractive surgery, pregnancy or nursing, or autoimmune disorders may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial evaluates the safety, efficacy, and patient satisfaction of three different techniques for correcting myopia: Small Incision Lenticule Extraction (SMILE), Implantable Collamer Lens (ICL), and the Wavelight Plus Alcon system. It aims to provide insights into how these methods compare in terms of outcomes for patients with myopia. Participants will be adults aged 18-40 with specific refractive error criteria, and the study will assess their experiences and results post-procedure.
Why it matters
Potential benefit: If successful, this study could help identify the most effective and satisfactory method for myopia correction, improving vision outcomes for patients.
How similar studies have gone: Other studies have shown success with similar refractive surgery techniques, but the comparison of these specific methods is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adults aged 18-40 years * Spherical equivalent of -1.00 to -10.00 D * Stable refraction for at least 12 months * Informed consent provided Exclusion Criteria: * Other ocular pathologies * Previous refractive surgery * Pregnancy or nursing * Autoimmune or connective tissue disorders
Where it's running
-
Beijing New Vision Eye Hospital
Beijing, China Recruiting -
Beijing Visionly Plus Eye Hospital
Beijing, China Recruiting
Study contacts
- Study coordinator: Peng ZHOU, M.D.
- Email: drzhoupeng@gmail.com
- Phone: +86-18801871108
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.