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Choroidal and Retinal Changes After RLRL Therapy in Diabetes and Diabetic Retinopathy

Primary Purpose

Diabetes Mellitus, Type 2, Diabetic Retinopathy

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
RLRL device
Sponsored by
The Second People's Hospital of Foshan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2 focused on measuring Repeated low-level red-light (RLRL) therapy, Choroidal thickness

Eligibility Criteria

35 Years - 55 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Aged 35-55 years Diagnosis of type 2 diabetes mellitus No DR or only mild non-proliferative DR (NPDR) assessed by baseline clinical ocular signs and 7-field fundus color photography Exclusion Criteria: Spherical equivalent (SE) ≤ -6.0 diopter or axial length ≥26 mm Patients with complications such as DME and retinal detachment History of ocular surgical operations Severe systemic diseases Those who could not cooperate with the examination for any reason Cognitive impairment or mental illness Patients with other ocular diseases

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Sham Comparator

    Arm Label

    RLRL of 100% intensity

    RLRL of 5% intensity

    Arm Description

    Participants will be treated with RLRL treatment (100% intensity) twice per day with an interval of at least 4 hours, each treatment last 3 minutes. Cross over arms after one month of use and one month of washout period.

    Participants will be treated with the sham device (5% intensity) twice per day with an interval of at least 4 hours, each treatment last 3 minutes. Cross over arms after one month of use and one month of washout period.

    Outcomes

    Primary Outcome Measures

    Changes in subfoveal choroidal thickness
    Changes in subfoveal choroidal thickness after 1-month RLRL treatment, which is measured by optical coherence tomography.

    Secondary Outcome Measures

    Changes in choroidal vascularity index
    Changes in choroidal vascularity index after 1-month RLRL treatment, which is measured by optical coherence tomography.
    Changes in OCTA-derived parameters of the choroid and retina
    Changes in OCTA-derived parameters of the choroid and retina after 1-month RLRL treatment
    Changes in DR grading
    Changes in DR grading after 1-month RLRL treatment

    Full Information

    First Posted
    March 6, 2023
    Last Updated
    April 14, 2023
    Sponsor
    The Second People's Hospital of Foshan
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05773209
    Brief Title
    Choroidal and Retinal Changes After RLRL Therapy in Diabetes and Diabetic Retinopathy
    Official Title
    Effect of Repeated Low-level Red-light (RLRL) Therapy on the Choroid and the Retina in Diabetes and Diabetic Retinopathy
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    April 30, 2023 (Anticipated)
    Primary Completion Date
    October 30, 2023 (Anticipated)
    Study Completion Date
    December 30, 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    The Second People's Hospital of Foshan

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The choroidal thickness was found to be thinner in diabetic eyes without retinopathy compared to healthy eyes, thus choroidal thickness might be an important parameter for the development of diabetic retinopathy in diabetic eyes without retinopathy. Repeated low-level red-light (RLRL) therapy is an emerging innovative and non-invasive treatment for a variety of eye diseases. Notably, RLRL was found to be effective in thickening choroidal thickness in a 1-year randomized controlled trial, indicating its potential in modulating blood flow in the fundus. This study aims to answer whether RLRL therapy can thicken choroidal thickness in adults with diabetes mellitus or diabetic retinopathy.
    Detailed Description
    The goal of this study is to investigate the effect of repeated low-level red-light (RLRL) therapy on the choroidal and retinal structures in diabetes mellitus and diabetic retinopathy. This study will be conducted with a prospective randomized cross-over design with a total follow-up of 3 months. The control group will use the sham device but with only 5% of the original device's power. Comprehensive ophthalmic examinations, including visual acuity, intraocular pressure, optical coherence tomography, optical coherence tomography angiography, slit lamp will be assesses at baseline and within the follow up

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Diabetes Mellitus, Type 2, Diabetic Retinopathy
    Keywords
    Repeated low-level red-light (RLRL) therapy, Choroidal thickness

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    58 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    RLRL of 100% intensity
    Arm Type
    Experimental
    Arm Description
    Participants will be treated with RLRL treatment (100% intensity) twice per day with an interval of at least 4 hours, each treatment last 3 minutes. Cross over arms after one month of use and one month of washout period.
    Arm Title
    RLRL of 5% intensity
    Arm Type
    Sham Comparator
    Arm Description
    Participants will be treated with the sham device (5% intensity) twice per day with an interval of at least 4 hours, each treatment last 3 minutes. Cross over arms after one month of use and one month of washout period.
    Intervention Type
    Device
    Intervention Name(s)
    RLRL device
    Intervention Description
    Crossover device (RLRL of 5% or 100% intensity - alternate to first group). Cross over arms after one month of use and one month of washout period.
    Primary Outcome Measure Information:
    Title
    Changes in subfoveal choroidal thickness
    Description
    Changes in subfoveal choroidal thickness after 1-month RLRL treatment, which is measured by optical coherence tomography.
    Time Frame
    1 month
    Secondary Outcome Measure Information:
    Title
    Changes in choroidal vascularity index
    Description
    Changes in choroidal vascularity index after 1-month RLRL treatment, which is measured by optical coherence tomography.
    Time Frame
    1 month
    Title
    Changes in OCTA-derived parameters of the choroid and retina
    Description
    Changes in OCTA-derived parameters of the choroid and retina after 1-month RLRL treatment
    Time Frame
    1 month
    Title
    Changes in DR grading
    Description
    Changes in DR grading after 1-month RLRL treatment
    Time Frame
    1 month

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    35 Years
    Maximum Age & Unit of Time
    55 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Aged 35-55 years Diagnosis of type 2 diabetes mellitus No DR or only mild non-proliferative DR (NPDR) assessed by baseline clinical ocular signs and 7-field fundus color photography Exclusion Criteria: Spherical equivalent (SE) ≤ -6.0 diopter or axial length ≥26 mm Patients with complications such as DME and retinal detachment History of ocular surgical operations Severe systemic diseases Those who could not cooperate with the examination for any reason Cognitive impairment or mental illness Patients with other ocular diseases
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Xiangbin Kong, PhD
    Phone
    +86075788032111
    Email
    xiangbin_kong@sina.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Cong Li, MD
    Email
    leoleelc@163.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Xiangbin Kong, PhD
    Organizational Affiliation
    The Second People's Hospital of Foshan, Guangdong Province,China
    Official's Role
    Study Chair

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    Not Provided

    Learn more about this trial

    Choroidal and Retinal Changes After RLRL Therapy in Diabetes and Diabetic Retinopathy

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