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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04013204
Other study ID # PUCRI-2019- EndoFIND-01
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 15, 2019
Est. completion date June 2024

Study information

Verified date March 2021
Source Peking University
Contact Huan LIU, MSc
Phone 15650783607
Email liuhuan07@bjmu.edu.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to systematically evaluate the clinical application value of vascular endothelial function examination in patients with non-obstructive coronary artery disease.


Description:

The study will be carried out in two stages. Phase I is mainly intended to evaluate the effects of vascular EFT on the prescription of doctors and the application rate of mid and long-term secondary prevention medication in patients. If the results are positive, the sample size and observation time will be further expanded in Phase II to evaluate its impact on the cardiovascular events of patients, as well as its cost-effectiveness.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date June 2024
Est. primary completion date December 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - 1. Age: 18 years or older; - 2. Patients with NOCAD defined by CT or CAG results of less than 50% occlusion; - 3. Having signed their written informed consent. Exclusion Criteria: - 1. Left ventricular ejection fraction = 50%; - 2. Serious endocrine diseases (severe hyperthyroidism, hypothyroidism); - 3. Severe liver diseases (jaundice hepatitis, liver cirrhosis, liver failure); - 4. Severe nephropathy (uremia, renal failure); - 5. Severe inflammatory diseases (severe infection, lupus erythematosus, etc.); - 6. Malignant tumor; - 7. Mental disorders or cognitive disorders; - 8. Participating in other interventional clinical trials; - 9. There are any other factors that the treating doctors think are not suitable for inclusion or completion of this study.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Endothelial function guided therapy
To evaluate the effect of integration of non invasive endothelial function test (EFT) as a routine test in increasing appropriate treatment to reduce cardiovascular risk including prescription of lipid, blood pressure and glucose lowering medications by physicians at the clinic for patients with non-obstructive coronary artery disease (NOCAD) and the effect of introducing EFT as a routine test in reducing clinical endpoint (major adverse cardiovascular events) among patients with non-obstructive coronary artery disease(NOCAD).

Locations

Country Name City State
China Peking University Shougang Hospital Beijing

Sponsors (3)

Lead Sponsor Collaborator
Peking University Mayo Clinic, Peking University Shougang Hospital

Country where clinical trial is conducted

China, 

References & Publications (1)

Hwang IC, Jeon JY, Kim Y, Kim HM, Yoon YE, Lee SP, Kim HK, Sohn DW, Sung J, Kim YJ. Association between Aspirin Therapy and Clinical Outcomes in Patients with Non-Obstructive Coronary Artery Disease: A Cohort Study. PLoS One. 2015 Jun 2;10(6):e0129584. doi: 10.1371/journal.pone.0129584. eCollection 2015. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Compliance rate of patients to physicians prescription The incidence number of patients compliance to guidelines based medical therapy with prescription of cholesterol, blood pressure and glucose lowering medications by physicians at clinic for patients with non-obstructive coronary artery disease. up to 30 months
Primary Total incidence number of Major Adverse Cardiovascular Events The incidence number of MACE(Major Adverse Cardiovascular Events) including total death, non-fatal AMI or stroke(including stroke revascularization). up to 54 months
Secondary Mean improvement of endothelial function The mean improvement in endothelial function from baseline to 12 months, estimated by RHI(Reactive Hyperemia Index). up to 30 months
Secondary Incidence number of Major Adverse Cardiovascular Events The incidence number of MACE(Major Adverse Cardiovascular Events) during 0 to 12 months up to 30 months
Secondary Reduction of lipid levels The reduction in lipid levels from baseline to 12 months up to 30 months
Secondary Reduction of blood pressure The reduction in blood pressure from baseline to 12 months up to 30 months
Secondary Compliance rate of patients with treatment target The percentage of patients with treatment target attained in terms of hypertension, diabetes, and dyslipidemia at 12 months after baseline. up to 30 months
Secondary Compliance rate of patients with appropriate prescription by physicians The percentage of patients with appropriate prescription of cholesterol, blood pressure and glucose lowering medications by physicians at 3, 6 and 12 months after baseline. up to 30 months
Secondary Compliance rate of patients with healthy life style The percentage of patients with healthy life style at 3, 6 and 12 months after baseline. The healthy life style is defined as having no smoking, physical activities with at least 3 times a week and 30 min per time, BMI<25 Kg/M2. up to 30 months
Secondary Cost-effectiveness rate of Endothelial Function Testing The cost-effectiveness incremental ratio of Endothelial Function Testing in reducing MACE(Major Adverse Cardiovascular Events) . up to 54 months
See also
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Terminated NCT03010423 - Efficacy Study of Oral Nicorandil on Improving Microvascular Function in Female Non-obstructive Coronary Artery Disease (CAD) Participants Phase 4
Completed NCT05738876 - Non Obstructive Versus Obstructive Coronary Artery Disease
Enrolling by invitation NCT05634031 - Imaging Coronary Microvascular Dysfunction (CMD) Study N/A