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Clinical Demonstration Study on the Treatment of Unstable Angina Pectoris with Traditional Chinese Medicine Ointment Massage Technique

Clinical Demonstration Study on the Treatment of Unstable Angina Pectoris with Traditional Chinese Medicine Ointment Massage Technique

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002373
Enrollment
Unknown
Registered
2025-12-06
Start date
2025-12-12
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

unstable angina pectoris

Interventions

treatment group:Chinese herbal ointment massage + Guideline-directed medical therapy
control group:Vaseline ointment for massage + Guideline-directed medical therapy

Sponsors

Xiyuan Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Meets diagnostic criteria for unstable angina pectoris; (2) Meets Traditional Chinese Medicine diagnostic criteria for cold stagnation and blood stasis syndrome; (3) CCS angina pectoris grade I–III; (4) Angina attacks occurring =2 times per week and =6 times per day; (5) Age 18–75 years, irrespective of gender; (6) Sign the informed consent form and voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: (1) Patients with severe congestive heart failure, uncontrolled hypertension grade 3 or higher, cardiomyopathy, severe valvular heart disease, malignant arrhythmias (such as rapid atrial fibrillation, atrial flutter, ventricular tachycardia, second-degree type II or third-degree atrioventricular block), or those with implanted pacemakers; (2) Chest tightness or pain caused by other systemic diseases such as severe cardiovascular neurosis, menopausal syndrome, or cervical spondylosis; (3) Patients with infectious diseases or acute contagious conditions; (4) Those with concurrent acute cerebrovascular disease, malignant tumors, or severe underlying liver/kidney disorders (ALT, AST = 3 times upper limit of normal; serum creatinine > 220 µmol/L in males, > 175 µmol/L in females) or hematopoietic system disorders; (5) Patients with severe skin lesions or dermatological conditions at the ointment application site, including infection, breaks, ulcers, or scars; (6) Patients with bleeding tendencies (e.g., hemophilia, allergic purpura); (7) Patients immediately following strenuous exercise, extreme fatigue, heavy meals, intoxication, or in a state of hunger; (8) Patients with allergy to medications or components used in the study, such as Vaseline and Huoxue Huayu Ointment; (9) Patients who have taken traditional Chinese medicine or Chinese patent medicine within 2 weeks prior to the trial; (10) Pregnant or lactating women; (11) Patients with cognitive impairment unable to undergo corresponding assessments; (12) Patients currently enrolled in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Improvement in Angina Symptoms;

Secondary

MeasureTime frame
ECG improvement efficacy rate;Efficacy of Traditional Chinese Medicine Syndrome Score;Seattle angina questionnaire;PHQ-9;GAD-7;Cardiovascular Composite Endpoint Events;hsCRP;IL-6;Platelet activation index;

Countries

china

Contacts

Public ContactJuan Tan

Xiyuan Hospital, China Academy of Chinese Medical Sciences

tanjuan1984gg@sina.com18911063538

Outcome results

None listed

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