- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03121326
The Study of Sarcopenia and Aging Biomarkers by the Metabolomics
May 17, 2017 updated by: Chang Gung Memorial Hospital
With the rapid growth of the global elderly population, the studies of the biomarkers of the sarcopenia and aging are under investigation in different ways.
The investigators use Metabolomics to explore the biomarkers of the sarcopenia and aging of the senior adults.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
Metabolomics is the emerging platform technology to address the complexity of a living system.
In translational research, metabolomics approaches may enable the detection of multiple disease risk factors and interactions, disease progression, and response of patients to a particular therapy with or without side effects.
Metabolomics may provide comprehensive information and improve diagnosis and prognosis which are particularly promising in human complex degenerative diseases.
The investigators use Metabolomics to explore the biomarkers of the sarcopenia and aging of the senior adults.
Study Type
Observational
Enrollment (Anticipated)
650
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
-
-
-
Taoyuan, Taiwan, 333
- Recruiting
- Chang Gung University
-
Contact:
- Mei-Ling Cheng, PhD
- Phone Number: 3650 886-3-2118800
- Email: chengm@mail.cgu.edu.tw
-
-
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
60 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
650 residents of the Chang Gung Health and Culture Village aged over 60.
Description
Inclusion Criteria:
- residents of the Chang Gung Health and Culture Village
- mostly independent and do not require nursing assistance
- capable of managing their daily living activities
- aged ≧ 60
Exclusion Criteria:
- None.
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
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The biomarkers of the sarcopenia and aging in senior adults.
Time Frame: one year
|
Metabolomics to explore the biomarkers of the sarcopenia and aging.
|
one year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Study Chair: Chih-Ming Lin, M.D., Chang Gung Memorial Hospital
- Principal Investigator: Mei-Ling Cheng, PhD, Chang Gung University
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 (Actual)
March 6, 2017
Primary Completion (Actual)
March 15, 2017
Study Completion (Anticipated)
December 31, 2017
Study Registration Dates
First Submitted
April 17, 2017
First Submitted That Met QC Criteria
April 19, 2017
First Posted (Actual)
April 20, 2017
Study Record Updates
Last Update Posted (Actual)
May 19, 2017
Last Update Submitted That Met QC Criteria
May 17, 2017
Last Verified
March 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201700245B0
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
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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