Skip to content

Study on the Clinical Efficacy and Evaluation of Qilian Jiedu Hubao Fang for the Treatment of Acute Ischemic Stroke

Study on the Clinical Efficacy and Evaluation of Qilian Jiedu Hubao Fang for the Treatment of Acute Ischemic Stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000100
Enrollment
Unknown
Registered
2026-01-17
Start date
2026-03-01
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Acute Ischemic Stroke

Interventions

Experimental Group:1. Qilian Detoxifying and Brain-Protecting Formula: Ingredients: 30g of Radix Astragali, 6g of Coptis, 10g of Acorus tatarinowii, 15g of Paeonia rubra, 9g of Earthworm, 9g of Impera
Control Group:Conventional Western medical treatment is carried out in accordance with the "Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2023," which mainly includes: an

Sponsors

Beijing University of Chinese Medicine Dongzhimen Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Meets the diagnostic criteria for apoplexy in traditional Chinese medicine and acute ischemic stroke in Western medicine; (2) Patient age is between 18 and 80 years (inclusive), and written informed consent is obtained from the patient and their family; (3) Onset of ischemic stroke is within 72 hours; (4) NIHSS score is between 4 and 18 (inclusive); (5) Syndrome is classified as Qi deficiency with phlegm-heat; (6) The subject has given informed consent and voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Exclude diseases such as intracranial hemorrhage, intracranial infections, intracranial tumors, moyamoya disease, vasculitis, and carotid artery dissection, which may cause significant narrowing or occlusion of large vessels; (2) Patients with posterior circulation ischemic stroke confirmed by imaging studies; (3) Patients with a baseline modified Rankin Scale (mRS) score = 2 points prior to the current episode; (4) Patients who received thrombolytic therapy within = 24 hours; (5) Patients with mental abnormalities or consciousness disorders who are unable to cooperate with examinations or physical assessments; (6) Patients who were unable to complete cranial MRI or other relevant tests due to various reasons, or who refused related investigations or follow-ups; (7) Patients with severe diseases of the heart, lungs, liver, kidneys, or other major organs; (8) Pregnant women, those planning pregnancy, or women in the lactation period; (9) Patients currently participating in other interventional clinical trials.

Design outcomes

Primary

MeasureTime frame
mRS Score;

Secondary

MeasureTime frame
NIHSS score;Traditional Chinese Medicine (TCM) Syndrome Scale;BI Score;

Countries

China

Contacts

Public ContactChen Xing, Cui Fangyuan

Beijing University of Chinese Medicine Dongzhimen Hospital

yeahchency@sina.com18610044016

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 7, 2026