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Search for abnormalities of fundus blood vessels in moyamoya disease

Search for abnormalities of fundus blood vessels in moyamoya disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs031200402
Enrollment
50
Registered
2021-03-08
Start date
2021-04-23
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Moyamoya disease Moyamoya disease

Interventions

For fluorescein fundus angiography, 500 mg of fluorescein (5 ml vial of aqueous solution containing 500 mg of fluorescein) and 25 mg of Ophthagreen (2 ml of blue indocyanine green) are dissolved in 2

Sponsors

Akiyama Hideo
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Moyamoya disease patient group 1) Patients diagnosed with moyamoya disease (regardless of stage) 2) Patients aged 20 years or older (regardless of gender) 3) Patients with no previous history of fundus vascular disease 4) Outpatients 5) Patients who have given written consent to participate in this study. Normal fundus group 1) Patients who have undergone general ophthalmologic examination (visual acuity test, refraction test, intraocular pressure test, anterior segment and fundus examination), fundus photography, retinal optical coherence tomography, retinal optical coherence angiography, and laser speckle flow graphing examination at our ophthalmology department. 2) Patients who do not have fundus lesions in one or both eyes based on the above tests. 3) Patients who are 20 years old or older (regardless of gender) 4) Outpatients

Exclusion criteria

Exclusion criteria: Moyamoya disease patient group 1) Patients with a history of hypersensitivity to fluorescein and indocyanine green 2) Patients with a history of iodine hypersensitivity 3) Patients with a history of other serious drug allergies 4) Narrow-angle eyes 5) Pregnant women and lactating women (6) Patients within 6 months of angina pectoris or myocardial infarction attack 7) Hepatic dysfunction 8) Patients with a history of stroke or cerebrovascular surgery within 6 months 9) Other patients who are judged by the physician to be inappropriate for the study. Normal fundus group (1) Patients who do not wish to cooperate in the research by disclosing the research information through opt-out

Design outcomes

Primary

MeasureTime frame
Prevalence of Retinal Vasculature Abnormalities in Patients with Moyamoya Disease on Fluorescence Fundus Angiography

Secondary

MeasureTime frame
Retinal blood vessel density, area of central fovea no-reflux area, subcentral foveal retinal thickness, and subcentral foveal choroidal thickness obtained from retinal optical coherence tomography and retinal optical coherence angiography will be compared between groups of patients with moyamoya disease and normal fundus.

Contacts

Public ContactHideo Akiyama

Gunma University Hospital

akiyamah47@gunma-u.ac.jp+81-27-220-8338

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026