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Clinical Trials/JPRN-jRCTs031200402
JPRN-jRCTs031200402
Recruiting
未知

Search for abnormalities of fundus blood vessels in moyamoya disease

Akiyama Hideo0 sites50 target enrollmentMarch 8, 2021

Overview

Phase
未知
Intervention
Not specified
Conditions
Moyamoya disease
Sponsor
Akiyama Hideo
Enrollment
50
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 8, 2021
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Akiyama Hideo

Eligibility 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)

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.

Outcomes

Primary Outcomes

Not specified

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