Trials / Unknown
UnknownNCT04946474
Clinical Evaluation of the Combination of Symptoms and Symptoms With General Treatment for Acute Hemorrhagic Stroke
Clinical Evaluation and Study on the Combination of Disease and Syndrome With General Treatment for Acute Hemorrhagic Stroke
- Status
- Unknown
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 520 (estimated)
- Sponsor
- Peking University Third Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
Objective To evaluate whether Xingnaojing injection combined with Naoxueshu oral liquid can significantly improve the clinical outcome of patients with intracerebral hemorrhage. Secondary objectives included to evaluate whether combined application of Xingnaojing injection and Naoxueshu oral liquid can promote hematoma absorption or reduce perihematoma cerebral edema in patients with intracerebral hemorrhage
Detailed description
Objective To evaluate whether Xingnaojing injection combined with Naoxueshu oral liquid can significantly improve the clinical outcome of patients with intracerebral hemorrhage. Secondary objectives included to evaluate whether combined application of Xingnaojing injection and Naoxueshu oral liquid can promote hematoma absorption or reduce perihematoma cerebral edema in patients with intracerebral hemorrhage Statistical Methods: The main effective outcomes will be based on a generalized linear model and adjusted for associated confounders.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Xingnaojing injection + Shuxuetong oral liquid | Xingnaojing injection (administered immediately after joining the group, once a day, treatment for 10 days) + Naoxueshu oral liquid treatment (administered on the 4th day of onset, 3 times a day, treatment for 30 days ). |
Timeline
- Start date
- 2019-06-01
- Primary completion
- 2020-07-01
- Completion
- 2021-09-01
- First posted
- 2021-06-30
- Last updated
- 2021-06-30
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT04946474. Inclusion in this directory is not an endorsement.