Skip to content

Use of comparative effectiveness research for similar Chinese patent medicine for angina pectoris of coronary heart diseases: a new approach based on patient-important outcomes

Comparative effectiveness evaluation method for personalization of Chinese patent medicines in clinical effect based on Patient Important Outcome

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TTRCC-14004406
Enrollment
Unknown
Registered
2014-03-23
Start date
2014-05-01
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

Pectoris of Coronary Heart Diseases

Interventions

1:Qishen Yiqi dropping pill + Fufang Danshen dropping
2:Fufang Danshen dropping pill+Qishen Yiqi dropping pill placebo

Sponsors

Institute of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Patients aged 40-75 years old; 2) Provision of signed informed consent; 3) Diagnosis of angina pectoris due to coronary heart diseases (stable angina, class I to III); 4) TCM pattern diagnosis of qi deficiency and blood stasis or qi and blood stasis.

Exclusion criteria

Exclusion criteria: 1) Patients below 40 or above 75 years old; 2) Diagnosis of NYHA class IV; 3) Uncontrolled class III hypertension (SP higher than 180mmHg and/or BP higher than 110mmHg); 4) Presence of severe arrhythmia; 5) Patients with serious primary hepatic, renal or hematologic illnesses, and with mental diseases or malignant tumors; 6) Presence of active peptic ulcer and other hemorrhagic diseases; 7) Pregnancy or lactation; 8) Patients with other complications who should not be included in the trial as judged by the recruiting personnel; 9) Patients with an allergic constitution or who has a history of allergy to the investigational drug; 10) Participation in another clinical trial either currently or within the last three months.

Design outcomes

Primary

MeasureTime frame
Improvement of the clinical symptoms;

Countries

China

Contacts

Public ContactCao Hongbo

Institute of Traditional Chinese Medicine, Tianjin University of Traditional Chinese Medicine

caohongboebm@foxmail.com+86 13752330880

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 7, 2026