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Clinical Study On The Relation Among Prescription, Syndrome and Disease of Turbid Phlegm and Blood Stasis for Coronary Heart Disease

Study on the Relation Between Syndrome and Disease of Turbid Phlegm and Blood Stasis for Coronary Heart Disease and Its Biological Basis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02526381
Enrollment
120
Registered
2015-08-18
Start date
2015-07-31
Completion date
2018-08-31
Last updated
2015-11-20

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

Conditions

Coronary Heart Disease

Brief summary

Clinical study on patients with turbid phlegm and blood stasis syndrome and Qi -Yin Deficiency syndrome of coronary artery disease (CHD) compared with normal cases will be launched. Detection of lipid metabolism, inflammation medium, endothelial cell injury, blood coagulation function evaluation of the relationship between disease and biochemical basis, detect plasma metabonomics and the gene expression profile chip, with phlegm - lipid metabolic disorder, stasis - microcirculation disorder, alternating knot - inflammation mediated and other system related to the biological basis. With Danlou Tablet for treatment, the investigators can observe result/effect index of turbid phlegm and blood stasis syndrome. Through comprehensive comparison of multi-level, multi-targets and multi-date biological index to discuss its sickness-syndrome-prescription corresponding relation and its biological basis.

Interventions

Five tablets of Danlou Tablets (1.5g) will be given three times a day in addition to regular western medications for the 8 weeks

DRUGTongmai Yangxin Pills

Forty pills of Tongmai Yangxin Pills (4g) will be given two times a day in addition to regular western medications for the 8 weeks

Sponsors

Tianjin University of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
35 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

1. Selecting people aged between 35 and 65; 2. Being up to the western diagnostic standard of chronic stable angina(complying with one or more of the following ): 1) There is a clear history of old myocardial infarction; 2) Have undergone coronary angiography or coronary Computed Tomography angiography(CTA) inspection hint antrum of coronary artery with at least a major branch pipe diameter stenosis≥50%; 3) Have received percutaneous coronary intervention (PCI) or Coronary Artery Bypass Grafting(CABG) treatment. 3. They should sign the informed consent.

Exclusion criteria

1. Had history of myocardial infarction or unstable angina, or coronary artery revascularization in 3 months.(coronary artery bypass graft or angioplasty); 2. With other diseases that might cause chest pain, including heart diseases, neurosis, menopausal syndrome,hyperthyroidism, Cervical vertebra sickness (arteria vertebrals and spinal cord), gastroesophageal reflux disease or hiatal hernia. 3. Using three or more of these drugs,namely beta blockers, calcium channel blockers, Energy metabolism drugs,and nitrate medications; 4. With hypertension and blood pressure after Anti-hypertensive Medical Therapy is still on the high side (systolic pressure ≥160 mmHg,diastolic pressure ≥100 mmHg)combined with severe cardiopulmonary insufficiency or severe arrhythmia (Rapid auricular fibrillation, atrial flutter or Paroxysmal Supra VentricularTachycardia); 5. Having liver disease or with unexplained serum transaminase continually increasing, or alanine aminotransferase(ALT) and aspartate aminotransferase (AST) greater than 2-fold of the upper limit of normal reference value; 6. Abnormal renal function; 7. Merger of hematopoietic system diseases, or a serious primary diseases such as malignant tumor; 8. Pregnant women, nursing mothers, or there is a requirement for fertility of women of childbearing age; 9. Diabetic kidney disease, severe gouty nephropathy and other metabolic diseases; 10. People with severe metabolic disease; 11. People who are expected with poor medical compliance or can't be visited on a regular basis; 12. Have participated in other clinical trials in recent 3 months; 13. Researchers considering there are other cases in which people are not suitable for attending the trial.

Design outcomes

Primary

MeasureTime frame
Traditional Chinese Medicine symptom scores of Turbid Phlegm and Blood Stasis for Coronary Heart Disease12 weeks
Seattle Angina Questionnaire12 weeks
The Short Form (36) Health Survey, (SF-36)12 weeks
Self-reporting Inventory(symptom checklist-90)12 weeks

Countries

China

Contacts

Primary ContactChunquan Yu, Dr.
ycq-4@163.com8622-59596309

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026