Wavelength Intervention for Nearsighted Kids
This study is looking into whether specialized soft contact lenses can help slow down nearsightedness (myopia) in children. Nearsightedness happens when the eye grows too long, and while glasses or contacts can fix blurry vision, they don't stop the eye from getting longer. This extra eye growth can lead to serious eye problems later in life. This study will compare two types of specialized soft contact lenses, called "specialized soft contact lens 1" and "specialized soft contact lens 2," to see if wearing them daily can slow down this eye growth. Researchers also want to understand how well children can wear these lenses and if there are any safety concerns. You might be able to join if you are between 7 and 12 years old, have a certain level of nearsightedness, and are willing to wear the lenses for at least 10 hours a day, six days a week.
- Study design
- This is an interventional study planning to enroll 80 participants. It is a randomized controlled clinical trial where participants will wear daily-use, daily-disposable soft contact lenses.
- What's involved
- Participants will wear specialized soft contact lenses for a minimum of 10 hours per day, at least six days a week, for one year. Measurements of refractive error and axial length will be taken at the start and after 12 months.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for 12 months, with primary endpoints measured at baseline and 12 months.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Wavelength Intervention for Nearsighted Kids
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Safal Khanal, OD, PhD · PRINCIPAL_INVESTIGATOR · Unversity of Alabama at Birmingham
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Inclusion
Exclusion
What this trial measures
- Change in cycloplegic spherical equivalent refractive errorBaseline and 12 months
Cycloplegic autorefraction measurements will be recorded using the WAM 5500 autorefractor in both eyes at baseline and follow-up visits. A set of 10 spherical equivalent measures will be obtained in each eye and later averaged to obtain the eye's final refractive error.
- Change in axial lengthBaseline and 12 months
Ocular component dimensions, including axial length, will be recorded using the Haag-Streit LenStar LS900 based on low-coherence interferometry. A set of five measurements in primary gaze in each eye will be averaged to obtain the final dimension of the ocular components.