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NCT05606237 · ClinicalTrials.gov registry record · NA

Efficacy of Repeated Low-level Red-light Therapy in Myopia Control

A NA study of Myopia, sponsored by University of California, San Francisco.

Recruiting
Registry status
NA
Development phase
90
Enrollment target
1
Study location

NCT05606237 is a NA study of Myopia that is actively recruiting participants, run by University of California, San Francisco. The registered enrollment target is 90 participants, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (66% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05606237, a NA study of Myopia, is actively recruiting participants, sponsored by University of California, San Francisco.

RECRUITING
Registry status
NA
Development phase
90 participants
Enrollment target
1
Study location

Study Summary

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.

Conditions Studied

Interventions

  • DEVICE Low-level Red Light Therapy Device

Study Locations (1)

California

  • University of California, San Francisco - San Francisco

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2023-07-14
Est. Completion 2027-01-14
Phase NA

What the Registry Record Tells You About NCT05606237

The ClinicalTrials.gov registry entry for NCT05606237 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 267-participant average among 90 other Myopia trials with a reported enrollment target (66% lower). The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Myopia appearing as the primary indexed condition, and to 1 intervention - of which Low-level Red Light Therapy Device is the first listed.

NCT05606237 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT05606237 about?

NCT05606237 is a clinical study titled "Efficacy of Repeated Low-level Red-light Therapy in Myopia Control". 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 ...

What is the current status of trial NCT05606237?

This trial is currently recruiting. It is a NA study. The enrollment target is 90 participants. The study started on 2023-07-14. Estimated completion is 2027-01-14.

What conditions does trial NCT05606237 study?

This clinical trial studies the following conditions: Myopia.

What interventions are being tested in trial NCT05606237?

The interventions under investigation include: Low-level Red Light Therapy Device (DEVICE).

Who is sponsoring clinical trial NCT05606237?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05606237 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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