Fact CheckerSign in

NCT07358052Completed

Current Status of Cardiovascular Diseases in Chinese Overweight/ Obesity Population: An Epidemiological Study (COPE)

Source: ClinicalTrials.gov · Last updated 22 Jan 2026

Brief summary (registry, in English)

This study is testing how overweight and obesity affect cardiovascular disease (CVD) prevalence, risk factors, and mortality among Chinese adults using nationally representative CCDRFS (China Chronic Disease and Risk Factor Surveillance) data. The purpose of the study is to characterize trends and determinants of CVD in adults with overweight or obesity and to quantify the excess mortality and population burden attributable to overweight/obesity. Participants will not receive any study medicine as this is an observational analysis of existing survey and mortality data. The study does not involve a new investigational drug; it analyses health and outcome data collected in routine practice and national surveys. The study will last for the duration needed to analyse the CCDRFS datasets and linked mortality follow-up.

Status (registry)
Completed
Study type
Observational
Enrollment
551931 (actual)
First submitted
24 Nov 2025
Start date
8 Dec 2025
Primary completion date
12 Dec 2025
Lead sponsor
Novo Nordisk A/S
Diseases
Obesity
NCT number
NCT07358052

What you commit to

  • Study type: Observational
  • Participants enrolled: 551931
  • From 8 Dec 2025 to the primary completion date, 12 Dec 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • \- Exclusion criteria include missing core baseline or follow-up data relevant to each part. The medical conditions under investigation include overweight and obesity, along with their comorbidity with CVD and associated risk factors.

Who the study is looking for

  • Signed consent obtained before any study-related activities (study-related activities are any procedure related to recording of data according to the protocol).
  • Male or female, age above or equal to 18 years at the time of signing informed consent.
  • Permanent residents (residing in the survey counties/cities/districts for ≥6 months) from the 2013, 2018, and 2023 CCDRFS surveys; With complete information from physical examinations, blood biochemical tests, and questionnaires, including:
  • Demographic information (age, sex, urban/rural classification, etc.);
  • Height, weight, waist circumference, blood pressure;
  • Blood biochemical indicators (fasting/2-hour postprandial blood glucose, glycated hemoglobin, lipid panel: high density lipoprotein cholesterol, low-density lipoprotein cholesterol, triglycerides, total cholesterol, serum creatinine, etc.);
  • Routine urine indicators: urine protein (or urine microalbumin); self-reported prevalence of CVD and major chronic diseases (e.g., hypertension, diabetes, dyslipidemia, etc.);
  • Major behavioral risk factors (smoking, alcohol consumption, physical activity, dietary patterns, etc.);
  • Information on concomitant medication use.

Age in the registry: 18 years to - · Sex: All

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
National Center for Chronic and Noncommunicable Disease Control and Prevention, Chinese CDC
Coordinator of this site? Confirm its status
BeijingChinaUnknown status
Novonordisk Facility
Coordinator of this site? Confirm its status
BeijingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.