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A Randomized Controlled Trial for Gualou Danshen Granules in the Treatment of Unstable Angina Pectoris Patients with Phlegm-Blood Stasis Syndrome

Gualou Danshen Granule on MicroRNA-155 and Its Target Gene Regulatory Network of Coronary Heart Disease

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000003201
Enrollment
Unknown
Registered
2020-04-10
Start date
2020-06-01
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

Unstable angina pectoris

Interventions

Sponsors

Guanganmen Hospital, Chinese Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Conforms to the diagnostic criteria of unstable angina pectoris in the guidelines for the diagnosis and treatment of unstable angina pectoris and non-st-segment elevation myocardial infarction published by the Chinese society of cardiovascular diseases. The diagnostic criteria of TCM syndromes are consistent with phlegm and blood stasis obstruction syndrome; (2) Patients with coronary heart disease confirmed by coronary angiography (1 or more major coronary artery stenosis degree >=50%); (3) Aged 35-75 years old; (4) Participate voluntarily in this clinical study and sign the informed consent form. Subjects should insist on taking the medicine for 4 weeks, complete the scale and test before and after treatment. A fixed contact way to complete the follow-up work is also requisite.

Exclusion criteria

Exclusion criteria: 1. Those who have been confirmed to have chest pain caused by stable angina pectoris, acute myocardial infarction, aortic dissection, other congenital heart disease, valvular disease, severe neurosis, etc .; 2. Poorly controlled hypertension (systolic blood pressure >=160mmHg or diastolic blood pressure >=100mmHg), severe cardiopulmonary dysfunction (heart function level III or IV); 3. Chest tightness and chest pain caused by arrhythmia; 4. Acute stage of cerebral infarction; 5. Patients with severe primary diseases such as liver, kidney, hematopoietic system, liver function ALT or AST value> 1.5 times the upper limit of normal value, those with abnormal renal function; 6. Those with acute infection within the last 2 weeks; 7. Combine with other serious diseases who must be treated (such as blood diseases, tumors, etc.); 8. Diabetes does not meet the general control standards, or more serious diabetes complications occur; 9. Women who are pregnant or breastfeeding; 10. Those with allergies or allergies to the test drug ingredients. In addition: 1) patients who are participating in other clinical trials or patients whose clinical trials are finished less than one month; 2) Researchers believe that other reasons are not suitable for clinical trials.

Design outcomes

Primary

MeasureTime frame
Phlegm-Blood Stasis Syndrome scoring criteria;Seattle Angina Scale score;Coronary Heart Disease Clinical Symptom Grading Scale;

Countries

China

Contacts

Public ContactHe Qingyong

Guang-An-Men Hospital, Chinese Academy of Chinese Medical Sciences

heqingyongg@163.com+86 010-83231289

Outcome results

None listed

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