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Suhexiang Pill for Acute Ischemic Stroke: A Registry Study (SUNRISE)

D

Dongzhimen Hospital, Beijing

Status

Enrolling

Conditions

Ischemic Stroke

Treatments

Drug: Suhexiang Pill

Study type

Observational

Funder types

Other

Identifiers

NCT05833932
2021XS-001-05

Details and patient eligibility

About

The primary purpose of this study is to investigate the effectiveness and safety of the Suhexiang Pill for patients with acute ischemic stroke in real-world settings.

Full description

Suhexiang Pill, a traditional Chinese patent medicine, is widely used in China for acute stroke. However, there is a lack of evidence of its efficacy and safety for acute ischemic stroke in real-world setting. This registry study will recruit 1000 patients who receive Suhexiang Pill treatment after acute ischemic stroke.

Enrollment

1,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Acute ischemic stroke within 7 days of symptom onset.
  • Age ≥ 18
  • Patient who has received Suhexiang Pill treatment
  • Patient or legally authorized representative has signed informed consent.

Exclusion criteria

  • Be allergic to Suhexiang Pill
  • Known to be pregnant or breastfeeding.
  • With conditions that render outcomes or follow-up unlikely to be assessed.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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