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The purpose of this study is to assess the effectiveness and safety of Qingre Huatan formula versus placebo on preventing early neurological deterioration in patients with acute ischemic stroke within 48 hours after onset.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Qingre Huatan Formula | Experimental | Patients will receive orally administered Qingre Huatan Formula, combined with guidelines-based standard care. |
|
| Qingre Huatan Formula placebo | Placebo Comparator | Patients will receive orally administered Qingre Huatan Formula placebo, combined with guidelines-based standard care. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Qingre Huatan Formula | Drug | Qingre Huatan Formula, granules, 1 bag each time, twice a day, orally, continue for 10 days. |
|
| Measure | Description | Time Frame |
|---|---|---|
| The incidence of early neurological deterioration within 7 days of onset | An increase of NIHSS ≥2 within 7 days of onset is considered as early neurological deterioration. The NIHSS (National Institute of Health Stroke Scale) is a neurological assessment tool for stroke patients, with scores ranging from 0 to 42. | Basline and Day 7 |
| Measure | Description | Time Frame |
|---|---|---|
| Change in National Institute of Health Stroke Scale scores from baseline to 10 days (after the treatment) | The NIHSS (National Institute of Health Stroke Scale) is a neurological assessment tool for stroke patients, with scores ranging from 0 to 42. Scores of 0-1 indicate near normal status, 1-4 mild stroke, 5-15 moderate stroke, 16-20 moderate-to-severe stroke, and 21-42 severe stroke. It is primarily used to quickly assess stroke severity and guide treatment decisions. |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Dongzhimen Hospital | Recruiting | Beijing | Beijing Municipality | 100700 | China |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 42051694 | Derived | Zheng X, Yang Z, Wu H, Zhao M, Que C, Xiong X, Mu Y, Zhang G, Kang L, Gao Y, Lai X. Efficacy and safety of Qingre Huatan Formula for the prevention of early neurological deterioration in patients with acute ischemic stroke (QUIET): rationale and design for a randomized double-blind placebo-controlled study. Front Med (Lausanne). 2026 Apr 13;13:1754648. doi: 10.3389/fmed.2026.1754648. eCollection 2026. |
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| ID | Term |
|---|---|
| D000083242 | Ischemic Stroke |
| ID | Term |
|---|---|
| D020521 | Stroke |
| D002561 | Cerebrovascular Disorders |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
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| Qingre Huatan Formula placebo | Drug | Qingre Huatan Formula placebo, granules, 1 bag each time, twice a day, orally, continue for 10 days. |
|
| Guidelines-based standard care | Other | Guidelines-based standard care for acute ischemic stroke |
|
| Basline and 10 days after treatment initiation |
| The proportion of patients with modified Rankin Scale score ≤2 on day 30 | The mRS (modified Rankin Scale) is an ordinal, graded interval scale that assigns patients among 7 global disability levels, which ranging from 0 (no symptom) to 5 (severe disability) and 6 (death). | Day 30 |
| The proportion of patients with modified Rankin Scale score ≤2 on day 90 | The mRS (modified Rankin Scale) is an ordinal, graded interval scale that assigns patients among 7 global disability levels, which ranging from 0 (no symptom) to 5 (severe disability) and 6 (death). | Day 90 |
| Activity of daily living of patients measured by Barthel Index score on day 30 | Barthel Index is a commonly used scale for measuring the activity of daily living of people. Score of 10-item scale ranges from 0 (worst) to 100 (best). | Day 30 |
| Activity of daily living of patients measured by Barthel Index score on day 90 | Barthel Index is a commonly used scale for measuring the activity of daily living of people. Score of 10-item scale ranges from 0 (worst) to 100 (best). | Day 90 |
| Incidence of treatment-related adverse events | Number of patients with any adverse events during the study. | 90 days after treatment initiation |
| D009422 |
| Nervous System Diseases |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |