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A Clinical Study on Shenxiang Suhe Pill for Treating Posterior Circulation Ischemic Vertigo

A Clinical Study on Shenxiang Suhe Pill for Treating Posterior Circulation Ischemic Vertigo

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077782
Enrollment
Unknown
Registered
2023-11-20
Start date
2021-03-01
Completion date
Unknown
Last updated
2023-11-27

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

Conditions

Posterior Circulation Ischemic Vertigo

Interventions

Control group:The control group was given aspirin enteric coated tablets (Bayer Medical and Health Co., Ltd., national drug approval number J20171021100 mg/tablet), with 1 tablet taken orally daily
Resuvastatin calcium tablets (AstraZeneca Pharmaceutical Co., Ltd., National Drug Approval J20120006, 10mg/tablet), taken orally once a night. Give symptomatic treatment to improve circulation and diz
Low-dose group:On the basis of the control group, the low-dose group received oral administration of Shenxiang Suhe Pills (Hangzhou Hu Qingyutang, National Medicine Approval Z33020141, 0.7g/bottle, 2
High-dose group:On the basis of the control group, the high-dose group received oral administration of Shenxiang Suhe Pills at a dose of 0.7g, once daily in the morning and evening.

Sponsors

Zhejiang Provincial Tongde Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1) Age: 40-85 years old; 2) Conforming to symptoms of posterior circulation ischemic dizziness; 3) TCD indicates abnormal hemodynamics of the vertebral basilar artery system; 4) Color Doppler ultrasound confirmed the existence of atherosclerotic plaque, lumen stenosis and occlusion in the vertebrobasilar artery system; 5) Head CT with/without brainstem, cerebellar, and occipital lobe infarction; 6) The patient or family member signs an informed consent form.

Exclusion criteria

Exclusion criteria: 1) Head CT indicates cerebral hemorrhage; 2) Severe liver and kidney function damage; 3) Malignant tumors; 4) Individuals with mental symptoms who are unable to cooperate.

Design outcomes

Primary

MeasureTime frame
Transcranial doppler;

Secondary

MeasureTime frame
Plasma viscosity;Total cholesterol;Low density lipoprotein cholesterol;High-density lipoprotein cholesterol;Triglyceride;CRP;Evaluation of dizziness efficacy;Scoring of Traditional Chinese Medicine Symptoms;

Countries

China

Contacts

Public ContactLin Xu

Zhejiang Provincial Tongde Hospital

27009782@qq.com+86 158 5828 9146

Outcome results

None listed

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