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Metabolomics and macrogenomics mechanism of Qi-zhi-xin-xiong phenomes of Xiong-bi-xin-tong

Metabolomics and macrogenomics mechanism of Qi-zhi-xin-xiong phenomes of Xiong-bi-xin-tong

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069259
Enrollment
Unknown
Registered
2023-03-10
Start date
2023-03-10
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Qi-zhi-xin-xiong phenomes of Xiong-bi-xin-tong

Interventions

Control group:Coronary heart disease routine western medicine standard treatment drug therapy(CHD)
Experimental group:Standard western medicine treatment for CHD as mentioned above combined with Chai-hu-shu-gan-san

Sponsors

The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Inclusion criteria for disease group: (1) In line with the traditional Chinese medicine industry standard of the People's Republic of China ''TCM Internal medicine Syndrome Diagnosis and Curative Effect Criteria'' (ZY/T001.1-94) TCM chest obstruction heartache qi stagnation cardiothoracic syndrome dialectical diagnosis basis, syndrome classification; Those who meet the diagnostic criteria of coronary heart disease and the diagnostic criteria of cardiac function grade I-II; (2) Those who meet the criteria for syndrome differentiation of chest obstruction, heartache, qi stagnation and cardiothoracic syndrome by 3 deputy director of traditional Chinese and Western medicine or above physicians; (3) Patients who meet the diagnostic criteria of coronary heart disease and the diagnostic criteria of cardiac function grade I-II; (4) Aged between 40 and 75 years (including 40 and 75); (5) Volunteer to participate in the experimental research and have signed the informed consent; (6) No intestinal infection within one month; Do not use antibiotics and probiotic preparations within one month, do not drink yogurt; (7) Have not taken similar proprietary Chinese medicine or traditional Chinese medicine decoction within one month; (8) The patient is informed and agrees to cooperate. 2. Inclusion criteria for the health group: (1) No gender limit, aged 40-75 years; (2) The syndrome differentiation of TCM constitution is peaceful quality; (3) No coronary heart disease, hypertension, kidney disease, tumor and other internal diseases; (4) The subject is informed and agrees to cooperate.

Exclusion criteria

Exclusion criteria: 1. Known allergy to test drug components; 2. Unable to cooperate, such as chest pain caused by other reasons; Coronary angiography or coronary CT results indicated that the main vessel (RCA, LM, LAD, LCX) was more than 75% stenosis; Severe heart valvular disease, pulmonary embolism, uncontrolled high blood pressure, and serious infections; Patients with severe diseases of liver and kidney, hematopoietic system and endocrine system; 3. Have a history of alcohol and drug abuse; 4. Patients who are participating in or have participated in other clinical trials within 12 weeks prior to the trial; 5. Pregnant or lactating patients or patients with fertility requirements; 6. Other patients should not participate according to the researcher.

Design outcomes

Primary

MeasureTime frame
Traditional Chinese Medicine Evidence Scale;Coronary heart disease laboratory indicators;

Secondary

MeasureTime frame
Coronary heart disease imaging;Seattle Angina Questionnaire, SAQ;Self-rating Depression Scale, SDS;Self-rating Anxiety Scale, SAS;Adverse event;

Countries

China

Contacts

Public ContactDuan Dayue

The Affiliated Traditional Chinese Medicine Hospital of Southwest Medical University

dduan@swmu.edu.cn+86 181 8189 3148

Outcome results

None listed

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