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OpenTrials
Completed

NCT Number: NCT03406234

Observational Study on a Chinese Population

An observational study was conducted in a health examination center to distinguish risk factors for health in a randomly recruited volunteers of Chinese population.

Completed

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Shenzhen Center for Chronic Disease Control

Shenzhen, Guangdong, 518020, China

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Han population, living in Shenzhen City for > 2 y, not in pregnancy, without hepatic diseases and renal diseases

Exclusion criteria

  • caught by organic diseases

Treatment and study plan

No intervention.

Other

Cross-sectional observation without interventions.

Primary outcomes

  1. Circulating 25OHD concentration.

    Time frame: Jan., 2014 - May., 2015

Secondary outcomes

  1. Body mass index

    Time frame: Jan.-Dec., 2013

  2. Plasma glucose

    Time frame: Jan.-Dec., 2013

  3. DNA polymorphisms

    Time frame: Jan., 2014 - Dec., 2017

  4. Plasma lipids

    Time frame: Jan.-Dec., 2013

  5. Blood pressure

    Time frame: Jan.-Dec., 2013

Sponsors and collaborators

Lead sponsor

Shenzhen Center for Chronic Disease Control

Other

Registry information

Official study title

Observational Study on the Risk Factors for Health in a Chinese Population

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Jan 23, 2018
Registry last updated
Jan 23, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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