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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05513794
Other study ID # qMT-PD-02
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 2, 2022
Est. completion date December 2023

Study information

Verified date August 2022
Source Heuron Inc.
Contact Yoomi Kim
Phone +82 032-429-8503
Email yoomi_kim@iheuron.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In order to develop an image analysis system that automatically detects and quantifies neuromelanin, this study aims to construct a database of a wide sample by collecting brain MRI neuromelanin images prospectively.


Recruitment information / eligibility

Status Recruiting
Enrollment 220
Est. completion date December 2023
Est. primary completion date August 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years and older
Eligibility Parkinsin group Inclusion Criteria: - Adults over 19 years old - Those who have clinically shown Parkinson's symptoms such as tremor, Rigidity, Bradykinesa and gait disturbance and are scheduled to take MRI scans - Dopamine transporter imaging shows a significant decrease in visual dopamine intake - A person who can read and understand the description and informed consent form - Upon hearing and fully understanding the detailed explanation of this clinical trial, a person who has voluntarily decided to participate and agreed in writing to comply with the precautions Exclusion Criteria: - Patient with a history of claustrophobia and mental illness; - Patient with metallic substances in the body - Any female subject who is likely to be pregnant who does not agree to contraception in a medically permitted manner during this clinical trial period - Pregnant or lactating women - Other cases where the investigator judged that it is difficult to participate in the study; Healthy volunteer group Inclusion Criteria: - Adults over 19 years old - A person who has no family history or diagnostic history of movement disorders; - A person with a score of 8 or higher on the CCSIT(cross cultural smell identification test) - A person with a score of 27 or higher on the MMSE Test - No Parkinson's symptoms on a neurological examination - Upon hearing and fully understanding the detailed explanation of this clinical trial, a person who has voluntarily decided to participate and agreed in writing to comply with the precautions Exclusion Criteria: - Patient with a history of central nervous system disease or cognitive disorder - Patient with a history of claustrophobia and mental illness; - Patient with metallic substances in the body - Any female subject who is likely to be pregnant who does not agree to contraception in a medically permitted manner during this clinical trial period - Pregnant or lactating women - Other cases where the investigator judged that it is difficult to participate in the study;

Study Design


Related Conditions & MeSH terms


Intervention

Device:
MRI Imaging
Neuromelanin sequence imaging

Locations

Country Name City State
Korea, Republic of Yong-in Severance Hospital, Yonsei University Health System Gyeonggi-do Yongin-si
Korea, Republic of Inje University Sanggye Paik Hospital Seoul Nowon-gu
Korea, Republic of Severance Hospital, Yonsei University Health System Seoul Seodaemun Gu

Sponsors (1)

Lead Sponsor Collaborator
Heuron Inc.

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Differences in Neuromelanin Volume by Age Descriptive Statistics for Neuromelanin Volume Measured by MRI Image by Age Within 1 weeks after enrollment
Secondary Differences in Neuromelanin Volume by group Descriptive Statistics for Neuromelanin Volume Measured by MRI Image by group Within 1 weeks after enrollment
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