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Clinical Trials/ITMCTR2200005923
ITMCTR2200005923
Not yet recruiting
Phase 1

Evidence-based clinical research on the intervention of activating blood circulation and removing toxicity herbs in patients with borderline coronary lesions

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Xiyuan Hospital of China Academy of Chinese Medical Sciences
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional study
Sex
Male

Investigators

Eligibility Criteria

Inclusion Criteria

  • (1\)Patients with coronary artery bordeline lesions confirmed by coronary angiography or coronary computed tomographic angiography with stenosis of at least one major coronary artery lumen between 50% and 70%;
  • (2\) Patients aged 18–80 years.
  • (3\) Patients with heart function grading of NYHA grade?\-?
  • (4\) Patients conform to the TCM standard of blood stasis syndrome
  • (5\) Patients will be informed about the trial and should voluntarily sign the consent form.

Exclusion Criteria

  • (1\) Patients who had previously undergone coronary stent implantation, coronary artery bypass grafting or acute myocardial infarction within 3 months;
  • (2\) Patients with diffuse lesions throughout the diseased vessels;
  • (3\) Those who had previously undergone other cardiac operations, such as valve replacement;
  • (4\) Patients with severe heart, liver and renal insufficiency, who are not suitable for coronary angiography and related examination and treatment;
  • (5\) Persons suffering from mental disorders;
  • (6\) Persons suffering from hepatitis, tuberculosis, AIDS and other infectious diseases;
  • (7\) Allergic constitution;
  • (8\) Pregnant and lactating women;
  • (9\) Those whose life expectancy is less than one year;
  • (10\) Participated in other clinical researchers within the last 3 months.

Outcomes

Primary Outcomes

Not specified

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