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Predictive Value of Non-fasting Blood Lipid Levels for Cardiovascular Events in Community Population(PICC Study)

Predictive Value of Non-fasting Blood Lipid Levels for Cardiovascular and Cerebrovascular Events in Community Population(PICC Study)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04212520
Enrollment
6500
Registered
2019-12-27
Start date
2020-01-01
Completion date
2050-12-31
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lipid

Keywords

non-fasting lipid, cardiovascular and cerebrovascular events, major adverse cardiovascular events

Brief summary

Numerous studies have shown that non-fasting blood lipid levels are closely related to the occurrence of cardiovascular and cerebrovascular events, but it is still unclear in the Chinese population. The purpose of the study is to investigate the association between non-fasting blood lipid levels and adverse outcomes in Chinese community population.

Detailed description

Study population includes subjects who living in community, of any race or ethnicity, 18 or older years of age, and have provided written informed consent to provide biological sample at one or more study visits. Physical examination, questionnaire survey and biological sample collection will be conducted at baseline and the incidence of a composite of major adverse cardiovascular events will be investigated during follow-up.

Interventions

OTHERNo intervention

No intervention

Sponsors

Guangdong Provincial People's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

•≥18 years old; * Signed informed consent; * Life expectancy is greater than 1 year.

Exclusion criteria

* mental disorder; * is not willing to participate in the clinical study; * suffered with other disease to quite the trial; * violated the protocol.

Design outcomes

Primary

MeasureTime frameDescription
All-cause mortalityThrough study completion, an average of 1 yearsAll-cause mortality was confirmed through a combination of hospital medical records, telephone contacts with patients or family members, and death registration at the Center for Disease Control and Prevention.
Cardiovascular MortalityThrough study completion, an average of 1 yearsCardiovascular mortality was defined as death attributable to an ischemic cardiovascular cause (including fatal cardiovascular events and stroke).
Cardiovascular and cerebrovascular diseasesThrough study completion, an average of 1 yearsThe number of and the incidence rate of cardiovascular and cerebrovascular diseases.

Countries

China

Contacts

Primary ContactFeng Ying-qing, PhD
651792209@qq.com+862083827812

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026