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NCT04453033Completed

DB RCT for Specialized Phototherapy in Parkinson's Disease.

Double-blind, Randomized Controlled Trial to Demonstrate Efficacy of Celeste® Specialized Phototherapy in Treating Parkinson's Disease.

Source: ClinicalTrials.gov · Last updated 17 Sept 2026

Brief summary (registry, in English)

This is a pivotal study to determine whether light therapy can improve non-motor and motor function in Parkinson's disease, on top of current best medical treatment.

Status (registry)
Completed
Study type
Interventional
Enrollment
350 (actual)
First submitted
26 Jun 2020
Start date
26 Feb 2024
Primary completion date
30 May 2026
Lead sponsor
PhotoPharmics, Inc.
NCT number
NCT04453033

What you commit to

  • Study type: Interventional
  • Participants enrolled: 350
  • From 26 Feb 2024 to the primary completion date, 30 May 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • An anticipated need for a change in dopamine replacement therapy, concomitant medications, OTC/supplements, or other alternative therapies during the participant's involvement in the investigation
  • History of previous light therapy use for PD

Other illness

  • Diagnosis of an atypical Parkinsonian syndrome

Other

  • Significant OFF state or bothersome dyskinesias that in the judgment of the rater, would interfere with participation in the study.
  • \-

Who the study is looking for

  • Diagnosis of Parkinson's disease as determined by the study PI, in keeping with the UK PD Society Brain Bank Criteria for the Diagnosis of PD
  • Responsiveness to dopaminergic medication, as judged by the rater, and have been using treatment for at least the past 1 year
  • Relatively good eyesight as attested to by participants (Corrective lenses of at least 20/60)
  • Stable levodopa and other anti-PD medications for at least 28 days prior to screening -

Age in the registry: 45 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Rochester
Coordinator of this site? Confirm its status
RochesterUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.