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Prospective randomized controlled trial study of Luofengning Granule in the treatment of unstable angina

Prospective randomized controlled trial study of Luofengning Granule in the treatment of unstable angina

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030533
Enrollment
Unknown
Registered
2020-03-06
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-03-09

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

Conditions

Unstable angina

Interventions

Sponsors

Xian Wang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Confirmed UA patients; 2. Aged 18 to 80 years; 3. No gender restriction; 4. According to the requirements of GCP, the subjects will sign the informed consent form knowingly and voluntarily.

Exclusion criteria

Exclusion criteria: 1. Patients with diagnosis of AMI, stroke or undergone PCI or coronary artery bypass grafting (CABG) within 1 month prior to enrollment; 2. Patients with coexistent severe heart failure (NYHA, Class IV) and severe arrhythmia (atrial fibrillation, atrial flutter, paroxysmal ventricular tachycardia, sinus bradycardia (heart rate = 160mmHg or diastolic blood pressure >= 100mmHg); 5. With the terminal phase cachexia of malignant tumors; 6. With high bleeding risk,such as history of hemorrage of vital organs (brain or upper gastrointestinal tract) within 6 months, low platelet counts, abnormal coagulation function, recent active hemorrhage,etc.; 7. Patients with bleeding tendency within 1 month after operation; 8. Women who are under breastfeeding, pregnant or preparing for pregnancy; 9. With poor compliance; 10. Patients with known or suspected allergy to the test drug or allergic constitution; 11. Patients who participate in any other clinical study or take any of its investigational drugs within the last three months.

Design outcomes

Secondary

MeasureTime frame
Seattle angina scale score;TCM syndrome;Myocardial nuclides;electrocardiogram;wall motion score index;C-reactive protein;IL-6;MMP-9;

Primary

MeasureTime frame
major adverse cardiac events;

Countries

China

Contacts

Public ContactXian Wang

Dongzhimen Hospital of Beijing University of traditional Chinese Medicine

dzmyywx@163.com+86 13901291371

Outcome results

None listed

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