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Clinical study of CCTA-FFRCT combined evaluation of coronary ischemia in early stage of coronary heart disease with traditional Chinese medicine

Scientific and technological innovation project of China Academy of Chinese Medical Sciences

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2022000025
Enrollment
Unknown
Registered
2022-06-17
Start date
2022-07-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

Stable Angina Pectoris of Coronary Heart Disease

Interventions

The test group:Chinese medicine and western medicine standard treatment
The control group:Western standard treatment for coronary heart disease

Sponsors

Guang 'anmen Hospital, Chinese Academy of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) It meets the diagnostic criteria of stable angina pectoris of coronary heart disease in Western medicine, and CTA shows that at least one major branch has a lumen diameter narrowing of 50%-75%; (2) 0.7 < FFRCT=0.8; (3) Meet the standard of TCM syndrome differentiation of chest obstruction and blood stasis; (4) Aged 18-85, with no gender limitation; (5) those who have not taken other Chinese herbs in the last two weeks; (6) Those who voluntarily participate and sign the informed consent of patients.

Exclusion criteria

Exclusion criteria: (1) Patients with a history of acute myocardial infarction in the last 3 months; (2) Patients with a history of serious arrhythmias, such as ventricular fibrillation, degree III ATrioventricular block, etc.; (3) Poor blood pressure control (systolic blood pressure =180mmHg or diastolic blood pressure =120mmHg); (4) serious diseases of liver, kidney, respiratory system, blood system, endocrine system and malignant tumors; (5) Women who are currently preparing for pregnancy, pregnancy or breastfeeding; (6) severe cardiac neurosis, perimenopausal syndrome, etc.; (7) patients suffering from mental disorders, or serious alcoholism and other adverse intoxication; (8) allergic to Chinese herbal medicine; (9) Incomplete medical records; (10) The researchers assessed other conditions for exclusion. Those who meet any of the above criteria will not be included in the test.

Design outcomes

Primary

MeasureTime frame
Noninvasive Fractional Flow Reserve Derived from Coronary CT;

Secondary

MeasureTime frame
TCM syndrome integral;Ultrasonic diastolic function parameter -- E/ e';

Countries

China

Contacts

Public ContactWu Huaqin
yuanshanyun2650@163.com13466679735

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026