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Clinical study on Wenyang Tongluo Decoction treating acute ischemic stroke (Yang deficiency syndrome)

Clinical study on Wenyang Tongluo Decoction treating acute ischemic stroke (Yang deficiency syndrome)

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076135
Enrollment
Unknown
Registered
2023-09-26
Start date
2023-10-01
Completion date
Unknown
Last updated
2023-10-03

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:Wenyang Tongluo Decoction
Control group:Warming Yang Tongluo placebo

Sponsors

Chongqing Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) meet the Western medicine diagnostic criteria for ischemic stroke and the Chinese medicine diagnostic criteria for stroke; (2) TCM syndrome differentiation is Yang deficiency syndrome; (3) Duration of onset =7 days; (4) 3 points =NIHSS=20 points; (5) Age =18 years old; (6) The patient or legal representative gives informed consent and signs the informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients who have received or plan to undergo intravascular interventional therapy (including arteriovenous thrombolysis, bridging, mechanical thrombectomy, angioplasty, and stenting); (2) There are major underlying diseases, serious liver or renal insufficiency (ALT or AST > 80u/l; Serum creatinine > 266umol/l (male), serum creatinine > 212umol/l (female)); (3) People with other non-cerebrovascular diseases caused by limb movement dysfunction; (4) other diseases or mental disorders that the investigator believes may limit the evaluation of neurological function or affect patient follow-up; (5) Pregnant or lactating women; (6) Those who are participating in clinical trials of other drugs; (7) There are contraindications for the drug therapy used in this study.

Design outcomes

Primary

MeasureTime frame
NIHSS score;

Secondary

MeasureTime frame
mRS;Barthel index;functional comprehensive assessment,FCA;TCM syndrome score;

Countries

China

Contacts

Public ContactJun Tang

Chongqing Hospital of Traditional Chinese Medicine

40621694@qq.com+86 137 0948 2548

Outcome results

None listed

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