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Clinical Trials List

Protocol Number202006173MINB
NCT Number(ClinicalTrials.gov Identfier)N/A

2021-01-01 - 2021-12-31

Others

Recruiting1

ICD-10I67.89

Other cerebrovascular disease

Investigating clinical features and biomarkers of parkinsonism in CADASIL patients

  • Trial Applicant

  • Sponsor

    National Taiwan University Hospital

  • Trial scale

    Taiwan Single Center

  • Update

    2025/08/20

Investigators and Locations

Principal Investigator CHIH-HAO CHEN Division of Neurology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Condition/Disease

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy(CADASIL)

Objectives

To investigate whether parkinsonism features, or vascular parkinsonism, is presented as an important clinical manifestation of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), and to identify relevant blood and neuroimaging biomarkers associated with parkinsonism in CADASIL.

Test Drug

13N-NH3

Active Ingredient

13N-NH3

Dosage Form

IVT

Dosage

37-74

Endpoints

To investigate the effects of plasma and nuclear imaging biomarkers on the parkinsonism features among CADASIL patients.
To elucidate potential application of 13N-ammonia PET on brain perfusion in cerebral small vessel disease.

Inclution Criteria

1) > 20 years old
2) with NOTCH3 mutation after genetic testing confirm

Exclusion Criteria

1) Due to contraindications or unable to cooperate with the MRI examination
2) Unable to cooperate with 13N-ammonia positron radiography (for example, unable to lie flat or have claustrophobia)
3) Pregnant women
4) People whose life expectancy does not exceed one year due to serious physical illness
5) Those who are not suitable for other factors evaluated by the doctor

The Estimated Number of Participants

  • Taiwan

    90 participants

  • Global

    90 participants