Last reviewed · How we verify
NCT05606237
Efficacy of Repeated Low-level Red-light Therapy in Myopia Control
NA trial testing Low-level Red Light Therapy Device in Myopia in 90 participants. Currently enrolling.
14 January 2027
Quick facts
| Lead sponsor | University of California, San Francisco |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 90 |
| Start date | 14 July 2023 |
| Primary completion | 14 January 2027 |
| Estimated completion | 14 January 2027 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Low-level Red Light Therapy Device
Conditions studied
- Myopia — all drugs for Myopia →
Sponsor
University of California, San Francisco
Who can join
Adults 8 to 13, any sex, with Myopia. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Low-level red-light technology provides a new and innovative myopia control approach. This strategy enables relatively high energies of light to be delivered at much shorter durations of exposure to induce the myopia control effect. The efficacy of the low-level red-light technology has been proven in a Chinese population. This trial demonstrated that 3-minutes per session twice a day repeated low-level red-light treatment controlled 87.7% of refraction progression and 76.8% of axial length elongation when the time of compliance to the treatment was 75%. Repeating this RCT in culturally diverse groups will confirm and translate this technology into a solution for myopia control globally.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Photobiomodulation Therapy: The Dawn of Myopia Control.
Gettinger K, Huang Y, Tsubota K, Negishi K, et al · · 2026 · PMID 41892317 · DOI 10.3390/cells15060526
Verify or expand the search:
- PubMed search for NCT05606237
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05606237 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of California, San Francisco
- Last refreshed: 28 January 2026
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05606237.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing