- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02917317
South China Prospective Cohort Study of Chronic Disease
September 12, 2017 updated by: Di Li, Sun Yat-sen University
To investigate the risk factors and prediction biomarkers of chronic disease in adults aged 35-74 years.
Study Overview
Status
Unknown
Conditions
Detailed Description
To investigate the risk factors and prediction biomarkers of chronic disease within adults aged 35-74 years in South China.
Following up the incidence of major chronic disease including stroke, coronary heart disease, cancer, chronic obstructive pulmonary disease, diabetes and hypertension.
Study Type
Observational
Enrollment (Anticipated)
110000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Fan J Hua, Ph.D
- Phone Number: 15626490788
- Email: fanjh3@mail2.sysu.edu.cn
Study Contact Backup
- Name: Xia Min, Ph.D
- Phone Number: 13650913974
- Email: xiamin@mail.sysu.edu.cn
Study Locations
-
-
Guangdong
-
Guangzhou, Guangdong, China, 510080
- Recruiting
- Guangdong Provincial Key Laboratory of Food, Nutrition and Health, Department of Nutrition, School of Public Health, Sun Yat-Sen University (Northern Campus)
-
Contact:
- Xia Min, PhD
- Phone Number: 0086 02087332433
- Email: xiamin@mail.sysu.edu.cn
-
Contact:
- Fan J Hua, PhD
- Phone Number: 0086 15626490788
- Email: fanjh3@mail2.sysu.edu.cn
-
Principal Investigator:
- Fan J Hua, PhD
-
-
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
35 years to 74 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
aged 35-74 years local residents or lived in local for 5 years more,no gender perfomance
Description
Inclusion Criteria:
aged 35-74 years local residents or lived in local for 5 years more
Exclusion Criteria:
Malignancy Cognitive impairment that can not cooperate with investigation
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 |
---|---|---|
Incidence of chronic disease
Time Frame: 4 years or more
|
Incidence of chronic disease, including stroke, coronary heart disease, cancer, chronic obstructive pulmonary disease, diabetes and hypertension
|
4 years or more
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Outcome of chronic disease
Time Frame: 4 years or more
|
Outcome and development of chronic disease
|
4 years or more
|
Death
Time Frame: 4 years or more
|
Death caused by chronic disease
|
4 years or more
|
Incidence of other disease
Time Frame: 4 years or more
|
Incidence of other disease,including hyperuricaemia,fatty liver disease and so on
|
4 years or more
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Fan J Hua, Ph.D, School of Public Health,Nutrition and Food Hygiene,Sun Yat-sen 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)
May 1, 2017
Primary Completion (Anticipated)
September 1, 2020
Study Completion (Anticipated)
December 31, 2020
Study Registration Dates
First Submitted
September 27, 2016
First Submitted That Met QC Criteria
September 27, 2016
First Posted (Estimate)
September 28, 2016
Study Record Updates
Last Update Posted (Actual)
September 13, 2017
Last Update Submitted That Met QC Criteria
September 12, 2017
Last Verified
September 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ZXYZM-5
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
IPD Plan Description
do not share participants data
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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