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A clinical study on Tanhuo decoction in the treatment of acute coronary syndrome combined with cerebral atherosclerosis in the elderly

A clinical study on Tanhuo decoction in the treatment of acute coronary syndrome combined with cerebral atherosclerosis in the elderly

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000068
Enrollment
Unknown
Registered
2026-01-13
Start date
2026-02-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Coronary Heart Disease

Interventions

Tanhuo decoction Group:Standard Western Treatment and Tanhuo decoction

Sponsors

Xuanwu Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: **Inclusion criteria:** 1. Patients with acute coronary syndrome who achieve hemodynamic stability within 24 hours after treatment; 2. A prior confirmed diagnosis of ischemic cerebrovascular disease, or =50% intracranial or extracranial arterial stenosis confirmed after admission by carotid ultrasonography and cerebrovascular ultrasonography; 3. Presence of manifestations consistent with the phlegm–heat syndrome, assessed based on tongue body, tongue coating, stool, mental state, facial appearance, breathing, presence/absence of fever, pulse characteristics, oral sensation, and urine. A weighted scoring system is applied to each item, and a total score =7 indicates phlegm–heat syndrome; 4. Age =60 years; 5. Either sex; 6. Provision of written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with persistent hemodynamic instability for >24 hours or hypotension related to acute coronary syndrome (blood pressure 5× the upper limit of normal, or creatinine clearance <30 mL/min/1.73 m²; 5. History of bronchial asthma; 6. Platelet count <80 × 10^9/L, or anemia (hemoglobin =100 g/L); 7. Contraindications to or allergy/hypersensitivity to aspirin, clopidogrel, ticagrelor, or statins; 8. History of malignancy; 9. Allergy to any components of traditional Chinese medicine.

Design outcomes

Primary

MeasureTime frame
White blood cell count;Neutrophil count;High-sensitivity C-reactive protein;Interleukin-6;

Secondary

MeasureTime frame
The incidence of major adverse cardiovascular and cerebrovascular events;

Countries

China

Contacts

Public ContactXia Jinggang

Xuanwu Hospital, Capital Medical University

xiajinggang@sina.cn13621041267

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 7, 2026