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Clinical Efficacy Evaluation of Sanqi Bingbu Formula in the Treatment of Ischemic Stroke Recovery Phase

Clinical Efficacy Evaluation of Sanqi Bingbu Formula in the Treatment of Ischemic Stroke Recovery Phase

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001606
Enrollment
Unknown
Registered
2026-06-26
Start date
2026-06-30
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Ischemic Stroke Recovery Phase

Interventions

Experimental Group (Sanqi Bingbu Formula Group):Conventional treatment + Sanqi Bingbu Formula decoction: Astragalus 30g, Codonopsis 15g, Cuscuta 15g, Angelica 10g, Chuanxiong 12g, Red Peony 12g, Earth
Control Group:Guideline-recommended conventional treatment: antiplatelet aggregation, lipid-lowering plaque stabilization medications, and standardized management of underlying conditions

Sponsors

Xiyuan Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Meet TCM and Western diagnostic criteria for ischemic stroke recovery phase, with Qi Deficiency Syndrome as primary TCM pattern (Qi Deficiency Score =7 points), may include other secondary patterns (2) 3 6 months prior and no significant residual neurological deficits; current episode is recurrent with typical symptoms

Exclusion criteria

Exclusion criteria: (1) Ischemic stroke secondary to special etiologies (tumor, trauma, hematological diseases, vasculitis, vascular malformations) (2) Comorbid severe conditions affecting outcome assessment (malignancy, cardiac dysfunction =NYHA III, respiratory failure, severe infections, severe anemia, uncontrolled thyroid dysfunction) (3) History of allergy/severe adverse reactions to trial drugs/excipients, or severe allergic constitution (4) Severe aphasia/cognitive impairment (MMSE <24) preventing comprehension/cooperation (5) Comorbid excess patterns (Liver Yang Hyperactivity, Phlegm-Heat Bowel Excess, Wind-Fire Disturbance) with pattern scores =7 (6) Recent use (1 month) of Qi-tonifying herbs/patents/health products (e.g., ginseng, astragalus, cordyceps, ginkgo, CoQ10) or Western medications potentially interfering with efficacy assessment (high-dose steroids, sedatives); participation in other clinical trials within 3 months (7) Pregnancy, lactation, or planned pregnancy within 6 months (8) Anticipated non-compliance with prescribed dosage/frequency/duration (9) Other conditions deemed unsuitable by investigators

Design outcomes

Primary

MeasureTime frame
Traditional Chinese Medicine Syndrome Score of Qi Deficiency in Stroke;

Secondary

MeasureTime frame
National Institutes of Health Stroke Scale;Disability Level (Modified Rankin Scale, mRS);Serum Adenosine Triphosphate Concentration;Serum Mitochondrial Respiratory Chain Complex IV;Multidimensional Fatigue Inventory ;Fugl-Meyer Assessment Scale;Activities of Daily Living (Barthel Index);Stroke-Specific Quality of Life Scale ;

Countries

China

Contacts

Public ContactTong Chenguang

Xiyuan Hospital of China Academy of Chinese Medical Sciences

xytcg@sina.com13910719053

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Aug 10, 2026