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A random, double-blind, single-simulation, placebo parallel controlled, multi-center clinical trial for Quick-acting Jiuxin Pill in the treatment of chronic stable angina (Qi stagnation and blood stasis syndrome)

A random, double-blind, single-simulation, placebo parallel controlled, multi-center clinical trial for Quick-acting Jiuxin Pill in the treatment of chronic stable angina (Qi stagnation and blood stasis syndrome)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021876
Enrollment
Unknown
Registered
2019-03-14
Start date
2019-04-30
Completion date
Unknown
Last updated
2019-03-18

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

Conditions

chronic stable angina (Qi stagnation and blood stasis syndrome)

Interventions

Case Group:Quick-acting Jiuxin Pill
Control Group:Simulator of Quick-acting Jiuxin Pill
open group:Quick-acting Jiuxin Pill

Sponsors

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Those who meet the diagnostic criteria of coronary heart disease; 2. It conforms to the diagnostic criteria of stable exertional angina pectoris (CSS angina severity grade I-III); 3. Patients with angina pectoris twice or more per week; 4. Those who accord with traditional Chinese medical syndrome discrimination of qi stagnation and blood stasis; 5. The aged 18 to 80 years. 6. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1) Myocardial infarction and moderate to severe heart failure occurred within 3 months; 2) Percutaneous coronary intervention or coronary artery bypass grafting or pacemaker implantation within 3 months; 3) Complicated with uncontrolled grade III hypertension (systolic blood pressure (> 180 mmHg) and/or diastolic blood pressure (> 110 mmHg), severe arrhythmia; 4) Chest pain caused by diseases other than coronary artery disease, such as psychosis, severe neurosis, hyperthyroidism, biliary heart syndrome, gastroesophageal reflux, aortic dissection, etc.; 5) The patients with liver, kidney, hematopoietic system and other serious diseases, including those with normal upper limit of ALT and AST > twice, and those with normal upper limit of serum creatinine (Scr) > 1.5 times 6) Anaphylaxis or allergic to the test drug ingredients; 7) Those who participated in other drug clinical trials within one month; 8) Researchers consider it inappropriate to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
The effect of angina pectoris ;;Incidence of cardiovascular events .;

Secondary

MeasureTime frame
Angina classification ;;Improvement of TCM syndromes ;;Seattle Angina Scale score;;The dosage of emergency drugs and the stopping rate ;;EKG efficacy.;

Countries

China

Contacts

Public ContactXiaolong Wang
wxlqy0214@163.com+86 13501991450

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 22, 2026