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A randomized, double-blind, placebo-controlled clinical trial about Xuesaitong Soft Capsule for treatment of coronary heart disease with blood stasis syndrome

The research on lncRNA-miRNA regulatory networks related to coronary heart disease with blood stasis syndrome

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800014980
Enrollment
Unknown
Registered
2018-02-26
Start date
2018-03-01
Completion date
Unknown
Last updated
2018-03-05

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

Conditions

Coronary heart disease

Interventions

Test group:Xuesaitong soft capsule + basic treatment

Sponsors

Guang'anmen Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 70 Years

Inclusion criteria

Inclusion criteria: follow the diagnostic criteria, aged 35-70 years old, and sign the informed consent

Exclusion criteria

Exclusion criteria: Stable angina;acute myocardial infarction; chest pain caused by congenital heart disease, valvular disease and severe neurosis; NYHA classification of cardiac function is III or IV; chest pain caused by arrhythmia; acute cerebral infarction; combined liver, kidney and blood system primary serious diseases; recent acute infection within 2 weeks; with other serious diseases and must be treated (such as cancer); uncontrolled diabetes, or with serious diabetic complications; mental disordered that could not complete questionnaires; pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
lncRNA;miRNA;mRNA;

Secondary

MeasureTime frame
Seattle Angina Questionnaiire;Questionnaire of coronary heart disease with blood stasis syndrome;Safety evaluation:incidence of adverse events,vital signs, ECG, myocardial enzymes, coagulation, blood lipids and other laboratory values;

Countries

China

Contacts

Public ContactJie Wang

Guang'anmen Hospital, China Academy of Chinese Medical Sciences

wangjie0103@126.com+86 010-88001238

Outcome results

None listed

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