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Clinical Efficacy of Qijin Dan in the Treatment of Unstable Angina Pectoris with Intermingled Phlegm and Blood Stasis Syndrome and Its Effects on the Expression of p53, GDF-15, and VEGF

Efficacy Observation and Mechanism Exploration of Qijin Dan in the Treatment of Unstable Angina Pectoris

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000900
Enrollment
Unknown
Registered
2026-04-03
Start date
2025-03-01
Completion date
Unknown
Last updated
2026-04-28

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

Conditions

Unstable angina pectoris

Interventions

Standard Western medicine treatment group:Western Standard Treatment
Qijin Dan group:Qijindan treatment in addition to standard Western medical therapy

Sponsors

Wuxi Traditional Chinese Medicine Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) A documented history of myocardial infarction, or coronary artery stenosis of = 50% confirmed via coronary angiography (CAG) or coronary computed tomography angiography (CCTA); with a concurrent Traditional Chinese Medicine (TCM) differentiation of Intermingled Phlegm and Blood Stasis Syndrome. (2) Stable vital signs and a sound general physical condition. (3) Aged between 18 and 80 years. (4) Voluntary provision of written informed consent prior to study enrollment.

Exclusion criteria

Exclusion criteria: (1) Patients diagnosed with other acute or severe cardiovascular conditions (e.g., severe arrhythmias, structural heart diseases), or concurrent acute systemic diseases including acute cerebral infarction and severe pulmonary insufficiency. (2) Patients presenting with severe heart failure, malignant tumors, or severe primary dysfunctions of the pulmonary, hepatic, renal, hematopoietic, or endocrine systems; as well as those with active gastrointestinal bleeding, gastric ulcers, or a bleeding diathesis that would preclude completion of the trial. (3) Patients with psychiatric disorders, severe cognitive impairment, or legally defined disabilities that prevent adequate informed consent or protocol adherence. (4) Women who are pregnant, lactating, or planning to conceive; or individuals with a known hypersensitivity to any components of the investigational drug. (5) Patients who are currently participating in, or have participated in, another clinical trial within the preceding three months. (6) Patients who refuse participation or are unwilling to comply with the study procedures. Patients meeting any one of the aforementioned criteria will be excluded from the study.

Design outcomes

Primary

MeasureTime frame
Tumor Protein p53;Growth differentiation factor15;Vascular endothelial growth factor;

Secondary

MeasureTime frame
Treatment efficacy of angina symptoms;Electrocardiogram efficacy;Seattle Angina Questionnaire (SAQ);Efficacy on TCM syndromes;Efficacy on blood stasis syndrome;Blood lipid levels;

Countries

China

Contacts

Public ContactShi Man

Wuxi Traditional Chinese Medicine Hospital

femm123@163.com18796600857

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: May 1, 2026