Repeated Low-Level Red-Light Therapy Shortens Axial Length

Eye Diseases Clinical Trial

Official title:

Repeated Low-level Red-light Therapy in High Myopia Children and Teenagers: a Prospective Single-arm Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05768152
• Other study ID #: (2022)-0131
• Status: Not yet recruiting
• Phase: N/A
• Start date: March 2023
• Est. completion date: May 2024

Study information

• Verified date: February 2023
• Source: The Second People's Hospital of Foshan
• Contact: Xiangbin Kong, MD, PhD
• Phone: +8613929994766
• Email: xiangbin_kong[@]sina.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this clinical trial is to investigate the incidence and magnitude of axial length shortening after repeated low-level red-light therapy in high myopia children and teenagers.

Description:

High myopia has become a major public concern globally, which is characterized by excessive axial elongation of the eyeball. Axial elongation is accompanied by mechanical stretching and thinning of the choroid and sclera, causing vision-threatening complications. Repeated low-level red-light (RLRL) therapy is an emerging effective and safe therapy for myopia control. Previous clinical trials in China have observed clinically significant axial shortening after RLRL treatment. The purpose of this study is to investigate and identify possible mechanism for axial length (AL) shortening after 12-month RLRL therapy in highly myopic children and teenagers aged 8-18 years. In addition to single vision spectacles, subjects will receive RLRL treatment at home under supervision of the parents/guardians according to a standard protocol. Axial length, visual acuity, cycloplegic spherical equivalent refraction, slit lamp, fundus camera and optical coherence tomography/angiography will be measured at 1-, 3-, 6- and 12-month follow-up visits.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 30
• Est. completion date: May 2024
• Est. primary completion date: May 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 8 Years to 18 Years

Eligibility

Inclusion Criteria:

1. Provision of consent.

2. Age: = 8 and = 18 years at enrolment.

3. High myopia: cycloplegic sphere of -6.00 diopters (D) or greater in both eyes.

4. Willing and able to participate in all required activities of the study.

5. The children currently on myopia control treatment can be recruited if myopia control treatments (including but not limited to atropine, orthokeratology, rigid gas-permeable lenses, defocus spectacles, etc.) are discontinued for at least 2 weeks.

6. Normal fundus, tessellated fundus or with peripapillary diffuse chorioretinal atrophy.

Exclusion Criteria:

1. Secondary myopia, such as a history of retinopathy of prematurity or neonatal problems, or syndromic myopia with a known genetic disease or connective tissue disorders, such as Stickler or Marfan syndrome.

2. Pathologic myopia with signs of macula-involving diffuse chorioretinal atrophy, patchy chorioretinal atrophy, macular atrophy, lacquer cracks, myopic choroidal neovascularization or Fuchs' spots.

3. Strabismus and binocular vision abnormalities in either eye.

4. Previous any intraocular surgery affecting refractive status.

5. Other reasons, including but not limited to ocular or other systemic abnormalities, that the physician may consider inappropriate for enrolment.

Related Conditions & MeSH terms

• Eye Diseases
• High Myopia
• Myopia

Intervention

Device:
• RLRL
RLRL will be performed twice per day with an interval of at least 4 hours, each treatment last 3 minutes, in addition to single vision spectacles with power for correcting distance refraction.

Locations

Country	Name	City	State
China	The Second People's Hospital of Foshan	Foshan	Guangdong

Sponsors (1)

Lead Sponsor	Collaborator
The Second People's Hospital of Foshan

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence rate of axial length shortening greater than 0.05 mm	Incidence rate of axial length shortening > 0.05 mm is characterized as the ratio of the number of participants whose axial length has shortened by greater than 0.05 mm to the total number of participants. Axial length (mm) is measured using the IOL Master.	12 months
Secondary	Incidence rates of axial length reduction greater than 0.10 mm and 0.20 mm	Incidence rates of axial length shortening > 0.10 mm and 0.20 mm are characterized as the ratio of the number of participants whose axial length has shortened by greater than 0.10 mm and 0.20 mm to the total number of participants. Axial length (mm) is measured using the IOL Master.	12 months
Secondary	Magnitude of axial length shortening among shortened eyes	The magnitude of axial length shortening is characterized as the amount of axial length reduction in eyes with axial shortening. Axial length (mm) is measured using the IOL Master.	12 months
Secondary	Changes in choroidal thickness (µm)	Changes in choroidal thickness are characterized as the difference between each follow-up visit and corresponding baseline values which are measured using the optical coherence tomography.	1, 3, 6 and 12 months
Secondary	Changes in axial length (mm)	Changes of axial length is characterized as the difference between each follow-up visit and baseline values which are measured using the IOL Master.	1, 3, 6 and 12 months
Secondary	Changes in corneal curvature (mm)	Changes of corneal curvature is characterized as the difference between each follow-up visit and baseline values which are measured using the IOL Master.	1, 3, 6 and 12 months
Secondary	Changes in anterior chamber depth (mm)	Changes of anterior chamber depth is characterized as the difference between each follow-up visit and baseline values which are measured using the IOL Master.	1, 3, 6 and 12 months
Secondary	Changes in white to white (mm)	Changes of white to white is characterized as the difference between each follow-up visit and baseline values which are measured using the IOL Master.	1, 3, 6 and 12 months
Secondary	Change of cycloplegic spherical equivalent refraction	Cycloplegic spherical equivalent change (Diopter, D) is characterized as the difference between each follow-up visit and baseline values. Refraction with full cycloplegia is performed with an autorefractor. The data on spherical and cylindrical power and axis is automatically extracted from the autorefractor. The spherical equivalent power (D) is calculated as the spherical power (D) plus half of the cylindrical power (D).	1, 3, 6 and 12 months
Secondary	Change of pathologic myopia fundus META-PM grading	The fundus images are classified based on META-PM classification system. Color fundus images are obtained using the fundus camera.	1, 3, 6 and 12 months
Secondary	Change in best corrected visual acuity	Best corrected visual acuity change is characterized as the difference between each follow-up visit and baseline values. Visual acuity is assessed using an Early Treatment Diabetic Retinopathy Study (ETDRS) chart with standard illumination at a distance of 4 meters.	1, 3, 6 and 12 months
Secondary	Incidence of self-reported adverse events	Incidence of self-reported adverse events is the rate of self-reported adverse events over a specified period for all the subjects. Subjects are asked to report any treatment-emergent adverse events, including but not limited to glare, flash blindness, and afterimages.	1, 3, 6 and 12 months