Condition or disease | Intervention/treatment |
---|---|
Dysglycemia Dyslipidemia | Other: No intervention |
Study Type : | Observational |
Actual Enrollment : | 1520 participants |
Observational Model: | Ecologic or Community |
Time Perspective: | Cross-Sectional |
Actual Study Start Date : | August 1, 2013 |
Actual Primary Completion Date : | November 30, 2013 |
Actual Study Completion Date : | December 31, 2014 |
Group/Cohort | Intervention/treatment |
---|---|
Cross-sectional
a cross-sectional study.
|
Other: No intervention
No intervention.
|
Ages Eligible for Study: | 20 Years to 85 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Probability Sample |
Inclusion Criteria:
Exclusion Criteria:
No Contacts or Locations Provided
Tracking Information | |||||
---|---|---|---|---|---|
First Submitted Date | June 26, 2019 | ||||
First Posted Date | July 1, 2019 | ||||
Last Update Posted Date | July 1, 2019 | ||||
Actual Study Start Date | August 1, 2013 | ||||
Actual Primary Completion Date | November 30, 2013 (Final data collection date for primary outcome measure) | ||||
Current Primary Outcome Measures |
|
||||
Original Primary Outcome Measures | Same as current | ||||
Change History | No Changes Posted | ||||
Current Secondary Outcome Measures |
|
||||
Original Secondary Outcome Measures | Same as current | ||||
Current Other Pre-specified Outcome Measures | Not Provided | ||||
Original Other Pre-specified Outcome Measures | Not Provided | ||||
Descriptive Information | |||||
Brief Title | Micronutrients and Health in Adult Chinese | ||||
Official Title | Not Provided | ||||
Brief Summary | Adult subjects were recruited from a health examination center. Their fasting blood samples were collected for laboratory analyses of multiple measures including mineral, glucose, lipids, etc. | ||||
Detailed Description | Not Provided | ||||
Study Type | Observational | ||||
Study Design | Observational Model: Ecologic or Community Time Perspective: Cross-Sectional |
||||
Target Follow-Up Duration | Not Provided | ||||
Biospecimen | Retention: Samples With DNA Description:
Blood samples were collected and separated by centrifugation for supernatant and blood cells.
|
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Sampling Method | Probability Sample | ||||
Study Population | Adult volunteers visiting a health examination center were randomly recruited with their consent to particiapate the study. | ||||
Condition |
|
||||
Intervention | Other: No intervention
No intervention.
|
||||
Study Groups/Cohorts | Cross-sectional
a cross-sectional study.
Intervention: Other: No intervention
|
||||
Publications * | Not Provided | ||||
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
|||||
Recruitment Information | |||||
Recruitment Status | Completed | ||||
Actual Enrollment |
1520 | ||||
Original Actual Enrollment | Same as current | ||||
Actual Study Completion Date | December 31, 2014 | ||||
Actual Primary Completion Date | November 30, 2013 (Final data collection date for primary outcome measure) | ||||
Eligibility Criteria |
Inclusion Criteria:
Exclusion Criteria:
|
||||
Sex/Gender |
|
||||
Ages | 20 Years to 85 Years (Adult, Older Adult) | ||||
Accepts Healthy Volunteers | Yes | ||||
Contacts | Contact information is only displayed when the study is recruiting subjects | ||||
Listed Location Countries | Not Provided | ||||
Removed Location Countries | |||||
Administrative Information | |||||
NCT Number | NCT04004143 | ||||
Other Study ID Numbers | QLS2014 | ||||
Has Data Monitoring Committee | Not Provided | ||||
U.S. FDA-regulated Product |
|
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IPD Sharing Statement | Not Provided | ||||
Responsible Party | Zhou Ji-Chang, Shenzhen Center for Chronic Disease Control | ||||
Study Sponsor | Shenzhen Center for Chronic Disease Control | ||||
Collaborators |
|
||||
Investigators | Not Provided | ||||
PRS Account | Shenzhen Center for Chronic Disease Control | ||||
Verification Date | June 2019 |