Home Monitoring of Diabetic Macular Edema

Sponsor
Zhongshan Ophthalmic Center, Sun Yat-sen University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05223569
Collaborator
(none)
120
2
15

Study Details

Study Description

Brief Summary

Diabetic macular edema (DME) is part of diabetic retinopathy (DR) and a leading cause of central visual loss in people with diabetes . Most patients require pharmacological inhibition using anti-vascular endothelial growth factor (VEGF) agents with multiple monitoring visits that include optical coherence tomography (OCT), visual acuity test, and multiple injections.The substantial visit frequency puts pressure on ophthalmic clinics, and can impose a tremendous burden on both patients and their caregivers. Therefore, self-service examination instruments that can be portable and fast-moving become the key for realizing Metaverse medicine. Recently, the investigators have developed a portable, self-administrated home OCT machine, which is designed for home-based OCT scanning and monitoring for patients with retinal diseases including DME, age related macular degeneration (AMD) and choroidal neovascularization (CNV) that require multiple anti-VEGF injections. The investigators have confirmed its image quality and validated the retinal thickness measurements obtained from this device by comparing with hospital OCT (staff-administrated and clinic-based).In this study, the investigators will conduct a randomized clinical trial (RCT) to compare the efficacy and cost-effectiveness of a Metaverse-assisted home OCT monitoring model versus standard hospital care model for patients with diabetic macular edema who need anti-VEGF injections.

Condition or Disease Intervention/Treatment Phase
  • Device: Metaverse-assisted home OCT monitoring model
  • Device: Hospital-based monitoring with a staff-administrated OCT
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Metaverse-assisted Home Monitoring of Diabetic Macular Edema
Anticipated Study Start Date :
Mar 1, 2022
Anticipated Primary Completion Date :
Jun 1, 2022
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Metaverse-assisted home OCT monitoring model

Participants will receive a home monitoring set, which includes a HoloLens2 headset, a self-administrated OCT, and a self-administrated smartphone-based visual acuity tester. For each home service, participants will undergo the following: HoloLens2-assisted online instruction provided by a virtual specialist Visual acuity self test using a smartphone Self-testing OCT imaging HoloLens2-assisted online consultation

Device: Metaverse-assisted home OCT monitoring model
A home monitoring set, which includes a HoloLens2 headset, a self-administrated OCT, and a self-administrated smartphone-based visual acuity tester

Active Comparator: Hospital-based monitoring with a staff-administrated OCT

Participants will be instructed to come back to the clinic to receive traditional OCT and VA examinations operated by the study coordinators every month.

Device: Hospital-based monitoring with a staff-administrated OCT
Participants come back to the clinic to receive traditional OCT and VA examinations operated by the study coordinators

Outcome Measures

Primary Outcome Measures

  1. Changes in visual acuity [12 weeks]

    Changes in visual acuity from baseline to 12 weeks adjusted for baseline visual acuity

Secondary Outcome Measures

  1. The costs of treatment [12 weeks]

    The Cost-effectiveness between the two monitoring models

  2. Number of intravitreal injections [12 weeks]

    The number of intravitreal injections given per group

  3. Gains or losses in visual acuity [12 weeks]

    The proportion of eyes with two- and three-line gains or losses in visual acuity

  4. Central subfield thickness change as measured by optical coherence tomography [12 weeks]

    central subfield thickness and retinal volume as measured by OCT after 12 weeks

  5. Number of visits [12 weeks]

    The number of visits during the study

  6. Changes in visual acuity after 24 weeks [24 weeks]

    Changes in visual acuity from baseline to 24 weeks adjusted for baseline visual acuity

  7. Changes in visual acuity after 48 weeks [48 weeks]

    Changes in visual acuity from baseline to 48 weeks adjusted for baseline visual acuity

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age ≥18 years;

  2. Diagnosis of diabetic macular edema:

  • Type 1 or type 2 diabetes mellitus;

  • Center-involved macular edema;

  1. Willing to receive anti-VEGF treatment;

  2. Media clarity, pupillary dilation, and individual cooperation sufficient for adequate OCT examination;

  3. Able to operate self-administratedhome OCT by themselves or with the help of family;

  4. Travel time from home to hospital: within 2 hours driving.

  5. Able and willing to provide informed consent.

Exclusion Criteria:
  1. History of systemic anti-VEGF or pro-VEGF treatment within 4 months prior to randomization. (These drugs should not be used during the study);

  2. History of corticosteroid treatment (intravitreal or peribulbar) at any time in the past 4 months;

  3. History of macular laser photocoagulation in the past 4 months;

  4. Macular edema due to reasons other than diabetes;

  5. Coexisting ocular diseases that might alter visual acuity during the course of the study, such as retinal vein or artery occlusion, uveitis or other ocular inflammatory disease, neovascular glaucoma, etc.);

  6. Hypertension (systolic blood pressure (BP) above 180 or diastolic BP above 110);

  7. History of myocardial infarction, other acute cardiac event requiring hospitalization, stroke, transient ischemic attack, or treatment for acute congestive heart failure within 4 months prior to randomization;

  8. Pregnant or lactating;

  9. Currently participating in other clinical trials;

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Zhongshan Ophthalmic Center, Sun Yat-sen University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Zhongshan Ophthalmic Center, Sun Yat-sen University
ClinicalTrials.gov Identifier:
NCT05223569
Other Study ID Numbers:
  • 2021KYPJ099
First Posted:
Feb 4, 2022
Last Update Posted:
Feb 4, 2022
Last Verified:
Feb 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 4, 2022