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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05833932
Other study ID # 2021XS-001-05
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 1, 2023
Est. completion date December 31, 2024

Study information

Verified date June 2024
Source Dongzhimen Hospital, Beijing
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 1000
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Suhexiang Pill
Suhexiang Pill is an approved traditional Chinese patent medicine.

Locations

Country Name City State
China Dongzhimen Hospital Beijing Beijing
China Dongzhimen Hospital Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Dongzhimen Hospital, Beijing

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Proportion of patients independent Proportion of patients independent is defined as the modified Rankin Scale score of 0, 1, or 2. 90 days
Secondary National Institute of Health Stroke Scale The National Institute of Health Stroke Scale (NIHSS) ranges from 0 to 42, with higher scores indicating more severe neurological deficits. The change from baseline to day 10 or discharge.
Secondary Glasgow Coma Scale The Glasgow Coma Scale (GCS) is used to describe the extent of impaired consciousness in all types of acute medical and trauma patients, ranging from 0 to 15, with lower scores indicating more severe impaired consciousness. The change from baseline to day 10 or discharge.
Secondary Patient reported outcome The patient reported outcome (PRO) scale of stroke consists of four dimensions including the influence on physical, emotional, and social functioning, as well as the overall satisfaction with treatment. At day 10 or discharge.
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