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NCT Number: NCT05431309

Role of Screening With Coronary Computed Tomography Angiography in Primary Prevention of Coronary Heart Disease

The primary objective of this study is to determine whether coronary computed tomography angiography (CCTA) -based coronary heart disease(CHD) prevention strategy will be superior to traditional CHD prevention strategy, in reducing the future risk of CHD which included myocardial infarction, angina, cardiac death, and an emergency/urgent coronary revascularisation procedure, in a community population aged 40 to 69 years with cardiovascular risk factors but no history of cardiovascular disease.

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Key information

Age range

40 year–69 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Recent studies found that the incidence of CAD, screening with CCTA, in the general population is as high as 42%~49%. However, the effectiveness of CCTA screening in the primary prevention of CHD is unclear. The investigators designed a randomized controlled, open-label, pragmatic study to determine whether coronary computed tomography angiography (CCTA) -based coronary heart disease(CHD) prevention strategy will be superior to traditional CHD prevention strategy.

Community volunteers aged 40 to 69 years who provide consent, and are eligible (with cardiovascular risk factors but no history of cardiovascular disease), will be randomized 1:1 to receive individualized primary prevention programs for CHD, including statin recommendation, based on CCTA results or traditional risk assessment results using the Chinese guideline on the primary prevention of cardiovascular diseases-recommended strategy. All subjects will be followed for 5 years, but until the target primary endpoint event is met. The primary composite outcome was the first occurrence of CHD, which included myocardial infarction, angina, cardiac death, and an emergency/urgent coronary revascularisation procedure.

In order to prepare the study with high quality, the investigators will performed a pilot study prior to the initiation of patient recruitment for the main study.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Resident population aged 40-69 in Nanjing, China
  • One or more of the following cardiovascular disease risk factors must be present, as follows:
  • Current or recent (within 12 months) smoker
  • Clinical diagnosis of hypertension (>140/90mmHg)
  • Hypercholesterolaemia (LDL≥4.1mmol/L or total cholesterol>6.0 mmol/L, including familial hypercholesterolaemia)
  • Diabetes mellitus
  • Rheumatoid arthritis
  • Systemic lupus erythematosus
  • Family history of premature cardiovascular disease (first degree relative with atherosclerotic cardiovascular disease, males, age<55 years; females, age<60 years)
  • Chronic kidney disease stage 3 (eGFR 30~59mL/min/1.73 m2)

Exclusion criteria

  • Plan to leave Nanjing within 5 years or be unable to complete the follow-up work
  • Refuse to sign informed consent or inability to understand and comply with the program process
  • Known atherosclerotic cardiovascular disease (eg. angina, coronary heart disease, stroke, transient ischemic attack, peripheral vascular disease)
  • Serious chronic kidney disease (eGFR< 30 ml/min/1.73 m2)
  • Serious liver disease or dysfunction (chronic active hepatitis and cirrhosis, or aspartate aminotransferase (AST) or alanine transaminase (ALT) > 3 times the upper limit of normal)
  • Prior coronary computed tomography angiography or invasive coronary angiography within the last 5 years
  • Not appropriate to be tested due to birth planning, allergies, acute thyroid storm, etc
  • Current use of statin therapy
  • Patients with diseases that seriously affect the survival period, such as malignant tumors
  • Other conditions at the discretion of the research group

Treatment and study plan

Coronary Computed Tomography Angiography

Diagnostic Test

Intervention strategies were selected according to CCTA results

standard treatment

Other

Traditional cardiovascular disease prevention strategy based on Chinese guideline

Primary outcomes

  1. The first occurrence of coronary heart disease

    Time frame: 5 years

    Composite of cardiac death, myocardial infarction, angina, and an emergency/urgent coronary revascularisation procedure.

Secondary outcomes

  1. Major cardiovascular adverse events (MACE)

    Time frame: 5 years

    Number of cardiac death, myocardial infarction, emergency/urgent coronary revascularisation procedure and stroke

  2. Death

    Time frame: 5 years

    Number of all-cause death, cardiovascular deaths, non-cardiovascular deaths and undetermined death

  3. Occurrence of serious adverse events related to iodinated contrast agent

    Time frame: 1 year

    Composite outcome: contrast-induced nephropathy and severe allergoid contrast agent reaction

  4. Coronary interventions

    Time frame: 5 years

    Number of invasive coronary angiography and coronary revascularisation procedures

  5. The primary end point(composite of cardiac death, myocardial infarction, angina, and an emergency/urgent coronary revascularisation procedure) in different subgroups

    Time frame: 5 years

    The primary end point(composite of cardiac death, myocardial infarction, angina, and an emergency/urgent coronary revascularisation procedure) will be analyzed in prespecified subgroups, including age, sex, diabetes, smoking status, hypertension, diabetes mellitus, hyperlipidemia, Chronic kidney disease stage 3

  6. Diet

    Time frame: at 1-year follow-up and final follow-up (5 years)

    Measured by Food Frequency Questionnaire

  7. Exercise

    Time frame: at 1-year follow-up and final follow-up (5 years)

    Change in activity levels measured through International Physical Activity Questionnaire(IPAQ)

  8. Smoking cessation

    Time frame: at 1-year follow-up and final follow-up (5 years)

    Proportion of patients who changed smoking habits (%)

  9. Change in cardiovascular risk factors (blood pressure)

    Time frame: at 1-year follow-up and final follow-up (5 years)

    Blood pressure(mmHg)

  10. Change in cardiovascular risk factors (lipids)

    Time frame: at 1-year follow-up and final follow-up (5 years)

    Lipids(mmol/L)

  11. Change in cardiovascular risk factors (body weight)

    Time frame: at 1-year follow-up and final follow-up (5 years)

    Body weight(kg)

  12. Change in cardiovascular risk factors(waist circumference)

    Time frame: at 1-year follow-up and final follow-up (5 years)

    Waist circumference(cm)

  13. Change in depression (PHQ-9)

    Time frame: at 1-year follow-up and final follow-up (5 years)

    Change in depression measured using Patient Health Questionnaire-9 (PHQ-9) instrument

  14. Change in anxiety (GAD-7)

    Time frame: at 1-year follow-up and final follow-up (5 years)

    Change in anxiety measured using Generalized Anxiety Disorder 7-item (GAD-7) instrument

  15. Change in quality of sleep(PSQI)

    Time frame: at 1-year follow-up and final follow-up (5 years)

    Change in quality of sleep measured using Pittsburgh Sleep Quality Index (PSQI) instrument

  16. Change in quality of life(SF-12)

    Time frame: at 1-year follow-up and final follow-up (5 years)

    Change in quality of quality of life measured using 12-item Short-Form Health Survey Questionnaire (SF-12) instrument

  17. Incidental findings in Computed Tomography Angiography group

    Time frame: at 1-year follow-up and final follow-up (5 years)

    Potential benefits and harms of the findings

  18. Medication adherence( anti-hypertension agent, hypoglycemic agent, antilipemic agents, anti-platelet, etc.)

    Time frame: at 1-year follow-up and final follow-up (5 years)

    Measure adherence using follow-up questionnaires (Whether participants are taking medication, why participants are not taking it or taking it, the name, frequency, dosage and side effects of the medication participants are taking)

  19. Health economics

    Time frame: 5 years

    Cost-Effectiveness analysis and Cost-Utility analysis

  20. Disadvantages of Radiation exposure

    Time frame: 5 years

    Radiation dose (mGy-cm)

Study contacts

Contact information is provided by the study sponsor or research team.

Longjiang Zhang, MD

CONTACT

[email protected]

+8613405833176

Sponsors and collaborators

Lead sponsor

Jinling Hospital, China

Other

Registry information

Official study title

Role of Screening With Coronary Computed Tomography Angiography in Primary Prevention of Coronary Heart Disease: a Community-based, Prospective Randomised Controlled Study

Acronym: RESPECT

Important dates

Study start
2022
Primary completion
2028
Study completion
2028
First posted
Jun 24, 2022
Registry last updated
Jul 7, 2022

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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