- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03909828
Precision Medical Diagnosis for Parkinson's Disease - The Quantitative Analysis System for PET/MRI Images in Patients
April 8, 2019 updated by: Taipei Veterans General Hospital, Taiwan
Precision Medical Diagnosis and Acupuncture Treatment for Parkinson's Disease - The Quantitative Analysis System for PET/MRI Images in Patients
In nuclear medicine PET examinations, labeled radiopharmaceuticals are possible to enter the putamen and caudate nucleus regions of the striatum in the brain by intravenous injection.
The severity of Parkinson's disease is assessed and diagnosed by quantitative analysis of the defect in the image of the radiopharmaceuticals. Clinical studies often use manual selection of regions of interest (ROIs) for quantitative analysis.
However, this method causes human error and low reproducibility due to subjective factors, and also considerable time consuming.
Therefore, in order to solve the above problems, this research project plans to build an automated quantitative analysis system for PET/MRI images.
The quantitative analysis of the PET images is performed automatically by using the putamen and caudate ROI segmented by the MRI images.
This automated quantitative analysis system is expected to improve the time-consuming, low reproducibility, and subjectivity problems of traditional manual ROI selection method, and provide a useful tool for the diagnosis of early PD.
In the first year, this sub-project is expected to perform MRI T1 and 18F-FDOPA PET scanning of before and after acupuncture-treated PD patients provided by sub-project 3.
In the second year, the correlation analysis will be made with the results of tremor test provided by sub-project 1 and that of the 99mTc-TRODAT SPECT image quantification provided by sub-project 4.
Study Overview
Status
Unknown
Conditions
Detailed Description
Parkinson's disease (PD) is a neurodegenerative disease whose pathogenic mechanism is the degeneration of substantia nigra of the midbrain, causing the degeneration of dopaminergic neurons in the putamen and caudate nucleus of the striatum, and the dopamine content in the synapses decreases and gradually loses the ability to act.
Most of the clinical symptoms are motor function defects.
The most obvious symptoms are tremor, limb stiffness, motor dysfunction and gait abnormality, and cognitive and behavioral problems may occur.
In nuclear medicine PET examinations, labeled radiopharmaceuticals are possible to enter the putamen and caudate nucleus regions of the striatum in the brain by intravenous injection.
The severity of Parkinson's disease is assessed and diagnosed by quantitative analysis of the defect in the image of the radiopharmaceuticals. Clinical studies often use manual selection of regions of interest (ROIs) for quantitative analysis.
However, this method causes human error and low reproducibility due to subjective factors, and also considerable time consuming.
Therefore, in order to solve the above problems, this research project plans to build an automated quantitative analysis system for PET/MRI images.
The quantitative analysis of the PET images is performed automatically by using the putamen and caudate ROI segmented by the MRI images.
In this study, patients will perform MRI T1 and 18F-FDOPA PET scanning of before and after acupuncture-treated PD patients in VGHTPE PET/MRI scanner.
Every patient will be administered 185 MBq (5 mCi) of 18F-FDOPA by IV injection.
The MRI image is used to extract the target and background ROIs (region of interests), and is coregistered to the PET image.
The ROIs generated by MRI image will be applied to its corresponding PET image.
Then, specific uptake ratio (SUR) will be calculated for each patient.
The calculation of SUR is the difference between the average image pixel value of the target ROI (left and right striatum) and the average image pixel value of the background ROI (occipital lobe) divided by the average value of the background ROI.
After calculated each patients' standard uptake ration, Asymmetry index (ASI) can be calculated based on the absolute difference of SUR value of both sides (left and right) of striatum, divided by average SUR value of both sides of striatum.
This automated quantitative analysis system is expected to improve the time-consuming, low reproducibility, and subjectivity problems of traditional manual ROI selection method, and provide a useful tool for the diagnosis of early PD.
In the first year, this sub-project is expected to perform MRI T1 and 18F-FDOPA PET scanning of before and after acupuncture-treated PD patients provided by sub-project 3.
In the second year, the correlation analysis will be made with the results of tremor test provided by sub-project 1 and that of the 99mTc-TRODAT SPECT image quantification provided by sub-project 4.
Study Type
Observational
Enrollment (Anticipated)
100
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The population consist of the participants who fulfill the inclusion criteria in eligibility criteria.
Description
Inclusion Criteria:
- Diagnosed as Idiopathic Parkinsonism by Neurologist
- Have taken first line drugs more than three months
- Did not take any acupuncture or rehabilitation
- Voluntary
Exclusion Criteria:
- Taking anticancer drug now or diagnosed as depression, psychosis or other mental illnesses
- Medical history of stroke or dementia
- Taking anticoagulant now or having coagulation disorders
- Scalp infection
- Pregnant women
- Patient with irregular heartbeat, implanted artificial cardiac pacemaker or implanted cardioverter-defibrillator
- Belonephobia
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Parkinson's disease patients
patients with Idiopathic Parkinsonism
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The comparison of the change of Standard Uptake Ration (SUR)
Time Frame: 2 Months
|
This study will collect images from a total of 100 PD patients (20 patients in the first year and 80 patients in the second year).
Patients will perform MRI T1 and 18F-FDOPA PET scanning of before and after acupuncture-treated PD patients in VGHTPE PET/MRI scanner.
Every patient will be administered 185 MBq (5 mCi) of 18F-FDOPA by IV injection.
The MRI image is used to extract the target and background ROIs (region of interests), and is coregistered to the PET image.
The ROIs generated by MRI image will be applied to its corresponding PET image.
Then, specific uptake ratio (SUR) will be calculated for each patient.
The calculation of SUR is the difference between the average image pixel value of the target ROI (left and right striatum) and the average image pixel value of the background ROI (occipital lobe) divided by the average value of the background ROI.The unit of pixel is mm and the unit of SUR measurement is percentage (%).
|
2 Months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Constitution in Chinese Medicine Questionnaire (CCMQ)
Time Frame: 2 Months
|
Sixty items were applied to measure the nine constitutions: Neutral (a normal constitution), Qi-deficiency constitution, Yang-deficiency constitution, Yin-deficiency constitution, Phlegm-dampness constitution, Damp-heat constitution, Stagnant-blood constitution, Stagnant-Qi constitution, and Inherited-special constitution.
|
2 Months
|
|
Sphygmograph
Time Frame: 2 Months
|
Diagnoses patient's pulse change
|
2 Months
|
|
The comparison of the change of asymmetry index (ASI)
Time Frame: 2 Months
|
After calculated each patients' standard uptake ration, Asymmetry index (ASI) can be calculated based on the absolute difference of SUR value of both sides (left and right) of striatum, divided by average SUR value of both sides of striatum.
The unit of ASI measurement is percentage (%).
|
2 Months
|
|
Unified Parkinson's Disease Rating Scale
Time Frame: 2 Months
|
A comprehensive assessment of both motor and non-motor symptoms associated with Parkinson's.
The Unified Parkinson's Disease Rating Scale is made up of 42 items.
These items are divided into six sections which are separately "evaluation of mentation, behavior, and mood", "self-evaluation of the activities of daily life", "clinician-scored monitored motor evaluation", "complications of therapy", "Hoehn and Yahr staging of severity of Parkinson's disease" and "Schwab and England ADL scale".The evaluation score for the first item to the 39th item is 0 to 4 points.
The evaluation score for the 40th to the 42th item is 0 to 1 points.
The higher score meand the worse condition.
The sum of all the items'score is the score of the scale.
Highr Rating Scales'scores indicate severe symptoms.
|
2 Months
|
|
Micro Vibration Scan
Time Frame: 2 Months
|
1. Discover early symptom before the onset. 2. Recognize PD tremor pattern within 1 minute. 3. Non-invasive, Non-radiation, and Low-cost medical device for daily tracking and treatment evaluation.
|
2 Months
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
statistical method-T test
Time Frame: 1 year
|
after all the measure, we will use T test as the statistical method to do data analysis
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ANTICIPATED)
April 1, 2019
Primary Completion (ANTICIPATED)
December 31, 2021
Study Completion (ANTICIPATED)
December 31, 2021
Study Registration Dates
First Submitted
January 22, 2019
First Submitted That Met QC Criteria
April 8, 2019
First Posted (ACTUAL)
April 10, 2019
Study Record Updates
Last Update Posted (ACTUAL)
April 10, 2019
Last Update Submitted That Met QC Criteria
April 8, 2019
Last Verified
April 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2018-10-001B
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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