- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01564316
Proteomics Study by Serum and Platelet With Neurodegeneration Disease Patients
April 14, 2016 updated by: Seoul National University Hospital
Using to method of Proteomics, for aims to conquer intractable disease, try to access variety experiment.
Biomarker is necessary to develop new diagnosis method and target of treatment.
Study Overview
Status
Terminated
Conditions
Detailed Description
Following Seoul National University Hospital Institutional Review Board approval, obtain serum and platelet with neurodegeneration patients and control group visited the part of neurology, there'll be analysis to differentiate each other diseases use to method Proteomics.
Biomarker will be screening via 1D/2D analysis, Mass analysis, database searching- the MASCOT search tool, SWISS-PROT and etc.
Study Type
Observational
Enrollment (Actual)
22
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Seoul, Korea, Republic of, 110744
- Department of Neurology, Seoul National University Hospital
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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
18 years to 80 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
neurodegeneration patients group include dementia patients visited the part of neurology.
(almost after diagnosis)
Description
Inclusion Criteria:
- neurodegeneration patients and control group include dementia patients visited the part of neurology.
- over the age of 18
- when participants can understand subject of this study
- Total point of Mini Mental state exam(MMSE)should be Under 26 include MCI (mild cognitive impairment) and over GDS score 3points.
exclusion criteria:
- under eighteen years of age
- when participants cannot understand subject of this study
- cannot accept this study
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 |
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neurodegeneration patients
•neurodegeneration patients and control group include dementia patients visited the part of neurology
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Manho Kim, Professor, Seoul National University Hospital
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
May 1, 2005
Primary Completion (Actual)
January 1, 2014
Study Completion (Actual)
January 1, 2014
Study Registration Dates
First Submitted
March 11, 2012
First Submitted That Met QC Criteria
March 23, 2012
First Posted (Estimate)
March 27, 2012
Study Record Updates
Last Update Posted (Estimate)
April 15, 2016
Last Update Submitted That Met QC Criteria
April 14, 2016
Last Verified
March 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H-0505-148-016
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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