Study of Photobiomodulation to Treat Dry Age-Related Macular Degeneration (LIGHTSITE1)

LumiThera

Status

Completed

Conditions

Age Related Macular Degeneration

Treatments

Device: LT-300 Active (PBM)

Device: LT-300 Inactive (Sham)

Study type

Interventional

Funder types

Industry

NIH

Identifiers

NCT02725762

1R43EY025508-01 (U.S. NIH Grant/Contract)

CSP001

Details and patient eligibility

About

The purpose of this research study is to determine if photobiomodulation is an effective treatment of Dry Age-Related Macular Degeneration (AMD) and vision loss associated with the disease.

Full description

The LumiThera LT 300® Light Delivery System is a stationary desktop instrument used to emit energy in the visible and near infrared spectrum. The LT-300® is designed for the ophthalmologist to use in the treatment of the eye with photobiomodulation (PBM), a process by which cellular mechanisms are induced by light. PBM is being utilized in many indications, such as wound healing, soft tissue injuries, joint pain, myofascial pain, nerve injuries, muscle fatigue for temporary improvement in blood flow and reduction in inflammation. The mechanism of PBM at the cellular level has been ascribed to the activation of mitochondrial respiratory chain components resulting in stabilization of metabolic function and initiation of a signaling cascade, which promotes cellular proliferation and cytoprotection. The LT-300® will provide a preset treatment of PBM to the subject's eye and retinal tissue through the open and closed eyelid.

Approximately 30 subjects meeting the eligibility requirements of the study will be randomly assigned in a 1:1 ratio to receive standard of care treatment for Dry AMD plus PBM treatment with the LT-300 system, or standard of care treatment for Dry AMD plus Sham treatment with the LT-300 system. Subjects randomized to each group will receive two 3-week treatment sessions (9 treatments per session) and follow-up visits extending to one year. The primary objective of the study is to evaluate the safety and efficacy of PBM with respect to visual and anatomical outcomes of subjects with Dry AMD.

Enrollment

30 patients

Sex

All

Ages

50+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients of both gender
Patients must have dry macular degeneration in the study eye
Best corrected visual acuity between 20/40 and 20/200
Patients must be competent to sign and have signed a consent form before study entry

Exclusion criteria

Visually significant cataracts.
Presence of a visually significant posterior capsule if prior cataract surgery has been performed.
Any visually significant disease process in any ocular structure that would affect vision unrelated to macular degeneration.
A patient can be enrolled if only one of their eyes meets the criteria. The other eye may be treated but not included in the study; for example advanced geographic atrophy.
Patients with severe clinically significant disease or unstable medical disorders including cardiovascular, hepatic, renal, neurological, endocrine, gastrointestinal, CNS or life threatening disease or current malignancy at the discretion of the investigators
Patients who are non-ambulatory or bed ridden
Female patients who are pregnant or of childbearing potential as effects of PBM on the developing human fetus are unknown.
Patients with a history of Epilepsy
Patients with a history of alcohol, drug or substance abuse in the past 6 months
Patients deemed uncooperative or non compliant with the requirements of the protocol.
Patients who have received any investigational drug or treatment within 30 days prior to study entry.
Patients who are not competent to understand and sign consent form.