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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01052350
Other study ID # 06-0706-201103106
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date August 2006
Est. completion date July 2030

Study information

Verified date December 2023
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to use a brain imaging method called PIB PET to determine dementia subtypes in patients with Parkinson's disease. The ultimate goal of this project is to be able to identify individuals with PD who are at risk of developing dementia, and to distinguish the underlying cause of dementia.


Description:

The purpose of this study is to use a brain imaging method called PIB PET to determine dementia subtypes in patients with Parkinson's disease. The ultimate goal of this project is to be able to identify individuals with PD who are at risk of developing dementia, and to distinguish the underlying cause of dementia. We will be including both PD and normal subjects in this study. This a long term study and we are considering including a total of 320 participants in this protocol.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 320
Est. completion date July 2030
Est. primary completion date July 2030
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 50 Years and older
Eligibility Inclusion Criteria: - PD patients must exhibit three of the following cardinal signs: rest tremor, rigidity, bradykinesia, or postural instability; or two of these features with one of the first three displaying asymmetry. Exclusion Criteria: - history of head trauma, major neurological or psychiatric diseases other than Parkinson disease and dementia, e.g. stroke, multiple sclerosis, depression or schizophrenia - severe systemic diseases - inability to lie still for 90 minutes - metallic implants, pacemakers, or any other contraindication to MRI - refusal to consent to brain donation

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States NeuroClinical Research Unit (NCRU), Washington University School of Medicine Saint Louis Missouri

Sponsors (1)

Lead Sponsor Collaborator
Washington University School of Medicine

Country where clinical trial is conducted

United States, 

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