跳至主要内容
临床试验/JPRN-jRCTs031220123
JPRN-jRCTs031220123招募中未知

Investigation for efficacy and safety of alpha-synuclein PET ligand [18F] C05-05

Endo Hironobu0 个研究点目标入组 91 人开始时间: 2022年6月9日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
91

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • (A) Brain dynamics evaluation
  • Patients (20 patients with dementia with Lewy bodies, 20 patients with Parkinsons disease, 10 patients with multiple system atrophy, 5 patients with progressive supranuclear palsy, 5 patients with corticobasal syndrome, and 5 patients with Alzheimers disease)
  • (1)Patients who are 20 years old or older at the time of consent acquisition.
  • (2)Patients whom a potential substitute can accompany on the day of participation in the study at QST
  • (3)Patients with dementia with Lewy bodies and Parkinsons disease: Patients who meet the UKPDSBB clinical diagnostic criteria or the diagnostic criteria of McKeith et al.
  • (4)Patients with multiple system atrophy: Patients who meet Gilmans clinical diagnosis criteria.
  • (5)patients with progressive supranuclear palsy: Patients who meet the diagnostic criteria of Hoeglinger et al and Kanazawa et al.
  • (6)patients with corticobasal syndrome: Patients who meet the clinical diagnostic criteria of Mayo and/or Cambridge.
  • (7)patients with Alzheimers disease: Patients who meet the NINCDS-ADRDA diagnostic criteria.
  • Healthy subjects (20 healthy subjects)
  • (1)Healthy adults who have been determined to be eligible for this study by the principal investigator or sub-investigator.
  • (2)Those who are 20 years of age or older at the time of obtaining consent.
  • (B) Whole body dynamic evaluation (6 Healthy subjects; 3 male and 3 female)
  • (1)Healthy adults who are judged to be eligible for this study by a medical examination by the principal investigator or sub-investigator.
  • (2)Healthy adults who are 50 years of age or older at the time consent is obtained.

排除标准

  • (1) Patients with a history of or complications from organic brain disease (for example, disorders of consciousness, head trauma requiring hospitalization, evident cerebral infarction, or cerebral hemorrhage).
  • (2) Patients with substance-related disorders (for example, drug dependence).
  • (3) Those who have complications from serious diseases or those who have a history of such diseases, judged by the principal investigator or sub-investigator to be inappropriate for this study.
  • (4) Those who have magnetic metals in their body (for example, tattoos, tattoos including art makeup, pacemakers) (for brain dynamics evaluation only).
  • (5) Persons with intense claustrophobia.
  • (6) Those who are pregnant or may be pregnant, and those who are breast-feeding.
  • (7) Those who are allergic to local anesthetics and blood coagulation inhibitors. (Brain dynamics evaluation only)
  • (8) Those who are taking the anticoagulant medication. (Brain dynamics evaluation only)
  • (9) Others judged by the principal investigator or sub-investigator to be inappropriate as research subjects.

研究者

发起方
Endo Hironobu

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