Skip to content

A multicenter randomized controlled clinical trial on the efficacy of Huatan Quyu Decoction in treating patients with acute ischemic stroke and fengtan zhiluo syndrome.

A Multicenter Randomized Controlled Clinical Trial on the Efficacy of Huatan Quyu Decoction for the Treatment of Acute Ischemic Stroke with Fengtan Zhiluo Syndrome.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000233
Enrollment
Unknown
Registered
2026-01-30
Start date
2026-01-30
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

acute ischemic stroke

Interventions

Experimental Group:Phlegm-Resolving and Stasis-Dispelling Formula + Guideline-Based Standardized Internal Medical Drug Therapy
Control Group:Evidence-based standardized internal medicine drug therapy.

Sponsors

Zhejiang Provincial Li Tongde Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1 )Meets the diagnostic criteria for acute ischemic stroke and corresponds to the traditional Chinese medicine syndrome type "wind-phlegm obstructing the meridians"; 2) Onset within 24 hours; 3) Age between 18 and 80 years (inclusive); 4) NIHSS score between 3 and 25 (inclusive); 5) Patient or legal representative has been informed and has signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients who have accepted or areto undergo intravenous thrombolysis or endovascular interventional therapy (including mechanical thrombectomy, arterial thrombolysis, and angioplasty); 2. Patients with stroke caused by brain tumors, brain trauma, or hematological diseases, as confirmed by examination; 3. Patients with a history of stroke and residual sequelae affecting outcome assessment, i.e., those with a pre-stroke mRS score =2; 4. Patients with atrial fibrillation, rheumatic heart disease, valvular heart disease, or other conditions that may lead to cardioembolic events; 5. Patients with conditions such as claudication, osteoarthritis, rheumatoid arthritis, or gouty arthritis that impair limb mobility and affect neurological examination; 6. Patients with severe liver or kidney dysfunction (Note: Liver dysfunction refers to ALT or AST levels greater than 2 times the upper limit of normal; kidney dysfunction refers to serum creatinine levels greater than 2 times the upper limit of normal); 7. Patients with other life-threatening severe diseases with an expected survival time of less than 3 months; 8. Patients with other diseases that may limit neurological function evaluation or affect follow-up; 9. Pregnant women, those planning pregnancy, or breastfeeding women; 10. Patients currently participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Modified Rankin Scale;

Secondary

MeasureTime frame
National Institutes of Health Stroke Scale (NIHSS);Glasgow Coma Scale;Barthel Index;

Countries

China

Contacts

Public ContactZhang Zhenzhong

Zhejiang Provincial Li Tongde Hospital

18758158548@163.com18758158548

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Mar 14, 2026