Registry of Amblyopia Patients Using Luminopia Treatment
Clinical Data Registry of Amblyopia Patients on Luminopia Treatment
Luminopia · NCT06429280
This study is looking at how well the Luminopia treatment works for people with amblyopia by collecting real-world experiences from patients and their eye doctors over at least 12 weeks.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 500 (estimated) |
| Sex | All |
| Sponsor | Luminopia (industry) |
| Locations | 13 sites (San Ramon, California and 12 other locations) |
| Trial ID | NCT06429280 on ClinicalTrials.gov |
What this trial studies
This observational study aims to collect real-world data on patients diagnosed with amblyopia who are undergoing Luminopia treatment, an FDA-approved therapy that utilizes a dual action dichoptic approach. The study will gather information on how ophthalmologists and optometrists are implementing this novel treatment in clinical practice. By analyzing the outcomes and experiences of patients over a minimum of 12 weeks of treatment, the study seeks to provide insights into the effectiveness and application of Luminopia in managing amblyopia.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals diagnosed with amblyopia who have been receiving Luminopia treatment for at least 12 weeks.
Not a fit: Patients who have participated in prior Luminopia clinical trials will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of Luminopia's effectiveness and improve treatment strategies for amblyopia.
How similar studies have performed: While this study is observational, previous studies on dichoptic treatments have shown promising results in managing amblyopia.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Have a diagnosis of amblyopia * Have undergone or currently undergoing Luminopia treatment for a minimum of 12 weeks Exclusion Criteria: -Have participated in prior Luminopia clinical trials
Where this trial is running
San Ramon, California and 12 other locations
- UCSF Benioff Children's Physicians — San Ramon, California, United States (RECRUITING)
- Sansum Clinic — Santa Barbara, California, United States (RECRUITING)
- Okaloosa Ophthalmology — Crestview, Florida, United States (RECRUITING)
- Family Focus Eye Care — Gainsville, Florida, United States (RECRUITING)
- Eye Physicians of Central Florida — Maitland, Florida, United States (RECRUITING)
- Children's Eye Institute of Savannah — Savannah, Georgia, United States (RECRUITING)
- Honolulu Eye Clinic — Honolulu, Hawaii, United States (RECRUITING)
- Lurie Children's Hospital — Chicago, Illinois, United States (RECRUITING)
- Riley Children's Hospital at IU Health — Indianapolis, Indiana, United States (RECRUITING)
- Nevada Eye Physicians — Las Vegas, Nevada, United States (RECRUITING)
- Concord Eye Center — Concord, New Hampshire, United States (RECRUITING)
- Children's Hospital Of Philadelphia — Philadelphia, Pennsylvania, United States (RECRUITING)
- Pediatric Eye Specialist — Fort Worth, Texas, United States (RECRUITING)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Amblyopia