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A clinical study about He Xue Tong Mai particles treating Phlegm and blood stenosis syndrome of angina pectoris combined with arterial atherosclerotic cerebral infarction

Research of TCM syndrome differentiation of Angina pectoris combined with arterial atherosclerotic cerebral infarction and Clinical study about He Xue Tong Mai particles treating Phlegm and blood stenosis syndrome of angina pectoris combined with arterial atherosclerotic cerebral infarction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003668
Enrollment
Unknown
Registered
2013-08-22
Start date
2010-09-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Angina pectoris combined with arterial atherosclerotic cerebral infarction

Interventions

Experimental group:He Xue Tong Mai particles
Control group:Placebo

Sponsors

Affiliated Hospital of Liaoning University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Comply with the diagnostic criteria of angina pectoris and atherosclerotic cerebral infarction (2 weeks -8 weeks) at the same time; 2. Comply with the diagnostic criteria of Phlegm and blood stenosis syndrome of angina pectoris combined with arterial atherosclerotic cerebral infarction; 3. The score of U.S. National Institutes of Health Stroke Scale (NIHSS) was >=5 points; 4. Aged from 35 to 85; Signed Informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with acute coronary syndrome (ST-segment elevation myocardial infarction, non-ST-segment elevation myocardial infarction, unstable angina, silent myocardial ischemia and ischemic cardiomyopathy; 2. Patients with rheumatic heart disease, hyperthyroidism, heart disease, myocarditis, cardiomyopathy, hypertension induced heart disease and other non-coronary atherosclerotic heart disease and cardiac neurosis; 3. In addition to atherosclerotic cerebral infarction of other reasons, such as arteritis, brain tumor, brain trauma, brain parasites, metabolic disorders, polycythemia vera, thromboembolism, intracranial vascular malformations, cerebral amyloidosis, etc; 4. Cerebral embolism, cerebral hemorrhage, transient ischemic attacks, lacunar infarction; 5. Patients associated with serious primary diseases of liver, kidney, hematopoietic system, malignant tumors, gastrointestinal bleeding and that were not expected to complete the trial; 6. Pregnant, breast-feeding women and Allergic people; 7. Patients with dementia, mental illness; 8. Patient with the rate of Modified Rankin Scale (MRS) of five (including unconsciousness) or Kubota water test >= 4 grade; 9. Canadian Cardiovascular Society (CCS) angina severity rating of 4; 10. People who participate in other clinical trials in two weeks; 11. Patients now use Chinese medicine which can promote blood circulation and dispel phlegm; Patient refused to sign the informed consent.

Design outcomes

Primary

MeasureTime frame
Syndromes (including clinical symptoms, signs, tongue, pulse);Angina Credits;Seattle angina questionnaire;NIH Stroke Scale;SS-QOL;ADL;Modified Rankin Scale;

Countries

China

Contacts

Public ContactGuanlin Yang

Liaoning University of Traditional Chinese Medicine

yanggl@lnzy.com+86 024 31207488

Outcome results

None listed

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