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A real-world study on the efficacy and safety of Xuesaitong soft capsule monotherapy vs. conventional antiplatelet therapy for ischemic stroke

A Retrospective Study on Xuesaitong Soft Capsules for Preventing Major Adverse Cardiovascular and Cerebrovascular Events in Ischemic Stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600123093
Enrollment
Unknown
Registered
2026-04-21
Start date
2023-11-01
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

ischemic stroke

Interventions

Observation group (treated with Xuesaitong Soft Capsules as monotherapy):None
Control group (treated with conventional chemical antiplatelet therapy):None

Sponsors

Dongfang Hospital, Beijing University of Chinese Medicine; Xuanwu Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Age = 18 years, gender (unrestricted). (2) First diagnosis of ischemic stroke between January 1, 2017, and December 31, 2021. (3) Within 1 year after diagnosis, cumulative use of any study drug from the specified regimens for at least 2 months, OR within 6 months after diagnosis, cumulative use for at least 1 month. The regimens are: Conventional antiplatelet therapy with oral chemical drugs (Aspirin and/or Clopidogrel, hereinafter referred to as Chemical Drug Therapy, Control Group I). Naoxintong Capsule combined with Chemical Drug Therapy (Control Group II). Tongxinluo Capsule combined with Chemical Drug Therapy (Control Group III). Xuesaitong Soft Capsule monotherapy (Observation Group I). Xuesaitong Soft Capsule combined with Chemical Drug Therapy (Observation Group II).

Exclusion criteria

Exclusion criteria: (1) History of using any study drug prior to the first diagnosis of ischemic stroke. (2) Comorbid malignant tumor(s). (3) Use of Xueshuantong Capsule, Compound Xueshuantong Capsule, or Sanqi Shutong Capsule for =2 months within 1 year after diagnosis. (4) Missing key study information (e.g., disease diagnosis, treatment records).

Design outcomes

Primary

MeasureTime frame
1-year cardiocerebrovascular composite events;

Secondary

MeasureTime frame
1-year all-cause mortality;

Countries

China

Contacts

Public ContactChen Zhigang

Dongfang Hospital, Beijing University of Chinese Medicine

chen_187588@126.com+86 180 8779 3053

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 1, 2026