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Clinical efficacy and endothelial function in acute coronary syndrome patients treated with Danhong Injection and Naoxintong capsule

Clinical efficacy and endothelial function in acute coronary syndrome patients treated with Danhong Injection and Naoxintong capsule:a randomized double-blind controlled trial.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-14005693
Enrollment
Unknown
Registered
2014-11-12
Start date
2014-12-19
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

Acute Coronary Syndrome

Interventions

The test group:Danhong Injection and Naoxintong capsule, conventional treatment of western medicine
The control group:Glucose Injection and placebo of Naoxintong capsule, conventional treatment of western medicine

Sponsors

Guangdong Provincal Hospital of Traditional Chinese medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Being in line with the Western standard of Acute Coronary Syndrome; 2. Fit with the TCM diagnosis of Qi deficiency and blood stasis and phlegm syndrome; 3. Patients who are aged between 30 to 75 yrs old, and have already signed the Consent form.

Exclusion criteria

Exclusion criteria: 1. People who has an allergy to Danhong injection or Naoxintong capsule; 2. People who are severe arrhythmia, such as type II second degree atrioventricular block, sick sinus syndrome (SSS), etc. and severe hypotension or hypertension, severe heart failure (above heart function lever III, and not under control), acute cardiac tamponade, and acute pulmonary oedema, etc.; 3. People who have any medical conditions like merge hemorrhage cerebrovascular accident (CVA), gastrointestinal bleeding, Diabetes complications or severe liver and kidney problems; 4. People who have any medical condition like hemophilia, severe thrombocytopenia, or dysfunction of blood coagulation; 5. People with cancer or mental illness; 6. People who need the Coronary Artery Bypass Grafting (CABG).

Design outcomes

Primary

MeasureTime frame
the incidence of cardiovascular events;

Secondary

MeasureTime frame
Endothelin, ET;Nitric oxide, NO;von Willebrand factor, vWF;flow mediated dilation, FMD;

Countries

China

Contacts

Public ContactBojun Chen
gzcbj@163.com+86 13902299108

Outcome results

None listed

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