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Evidence-based Optimization Study for TCM Syndrome Differentiation and Treatment Protocol of Stable Angina

Evidence-based Optimization Study for TCM Syndrome Differentiation and Treatment Protocol of Stable Angina

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR1900002386
Enrollment
Unknown
Registered
2019-06-08
Start date
2019-06-04
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

Experimental group:Dan Lou tablet flavoring combined with conventional western medicine treatment
Control group:Conventional western medicine treatment

Sponsors

Liao'ning University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of Western medicine 2.4(2) Diagnostic criteria for stable angina, Diagnostic criteria for chest bi-syndrome with the syndrome of turbid phlegm and blood stasis and have no conflict with the efficacy of Danlou tablets; 2. Aged from 35-75 years old; 3. Those who have not taken any TCM preparation within two weeks; 4. Those who can provide personal contact information and cooperate with the clinical trial visit and follow-up; 5. Those who voluntarily participate in clinical observations and sign informed consent form.

Exclusion criteria

Exclusion criteria: 1. Stable angina complicated with valvular heart disease, various types of cardiomyopathy, malignant arrhythmia; The patients with heart failure whose NYHA cardiac function grading is III-IV; 2. Stable angina complicated with hypertension without treatment or uncontrolled hypertension (Bp=180/110mmHg); 3. Stable angina complicated with severe cerebrovascular disease; 4. Stable angina complicated with severe pulmonary insufficiency (PaO2<60mmHg), endocrine and hematopoietic systems severe primary disease, Moderate to severe hepatic insufficiency(Transaminase levels are 3 times higher than the upper limit of normal) or Moderate to severe renal insufficiency(eGFR<60ml/min/1.73m2) or patients with newly diagnosed acute; 5. Stable angina complicated with cerebrovascular disease during the past 3 months; 6. Stable angina complicated with psychosis; 7. Stable angina patient who are in the period of gestation or lactation; 8. Stable angina patient participated in other clinical trials in the past 3 months; 9. Patient with a life expectancy lower than 1 year; 10. Allergic patients or patients who are allergic to TCM treatment; 11. Those who are unwilling or unable to accept clinical follow-up.

Design outcomes

Primary

MeasureTime frame
Frequency of angina pectoris;

Secondary

MeasureTime frame
Electrocardiogram;Serum differential endogenous products;MMP-9;Hemorheology;Echocardiography;Ang I;Exercise test;Seattle Angina Questionnaire;MPO;VCAM-1;IL-6;Hcy;Score of TCM symptoms;Anginal frequency;Blood glucose;Hs-CRP;Blood fat;Four coagulation;

Countries

China

Contacts

Public ContactZhang Mingxue

Liao'ning University of Traditional Chinese Medicine

zhmx6228@163.com+86 13998896592

Outcome results

None listed

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