Articles

Articles

Articles

The following information is intended for healthcare professionals only.

Below are links to published peer-reviewed articles featuring data from LumiThera-sponsored clinical trials, investigator-sponsored clinical trials, and photobiomodulation clinical trials.

The articles may contain information about treatments, populations, or uses that are not consistent with Valeda labeling or not approved by a regulatory authority. This is not a comprehensive or exhaustive list.

LumiThera does not suggest or recommend the use of its products in any manner other than as described in the Indications for Use in the Valeda User Manual.

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The Valeda Light Delivery System is intended to provide improved visual acuity in patients with best corrected visual acuity of 20/32 through 20/70 and who have dry age-related macular degeneration (AMD) characterized by:

  • The presence of at least 3 medium drusen {> 63 μm and ≤ 125 μm in diameter), or large drusen {> 125μm in diameter), or non-central geographic atrophy, AND
  • The absence of neovascular maculopathy or center-involving geographic atrophy

After about two years, the Valeda Light Delivery System treatment provides improved mean visual acuity of approximately one line of visual acuity (ETDRS) compared to those not receiving the treatment.

As a precaution, patients have not been tested and should not be treated with Valeda if they have any known photosensitivity to yellow light, red light or near-infrared radiation (NIR), or if they have a history of light activated central nervous system disorders (e.g. epilepsy, migraine). In addition, patients should not receive treatment within 30 days of using photosensitizing agents (e.g. topicals, injectables) that are affected by 590, 660, and/or 850 nm light before consulting with their physician.

Refer to the Valeda Light Delivery System User Manual for full Important Safety Information.

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