Trials / Completed
CompletedNCT03238742
The Efficacy of Xuebijing Injection on Sepsis
The Efficacy of Xuebijing Injection in Adult Patients With Sepsis
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 1,817 (actual)
- Sponsor
- Southeast University, China · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The Efficacy of Xuebijing Injection in Adult Patients with Sepsis
Detailed description
The purpose of this placebo-controlled study is to determine if Xuebijing Injection treatment provides significant mortality reduction improvement in patients with sepsis compared with placebo treatment in patients receiving the current standard of care for sepsis. This study will also assess the effectiveness of Xuebijing Injection in reducing 28-day mortality in patients with sepsis.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Xuebijing Injection | 100ml Xuebijing Injection every 12 hours for 5 days |
| DRUG | normal saline | 200ml normal saline every 12 hours for 5 days |
Timeline
- Start date
- 2017-10-20
- Primary completion
- 2019-07-28
- Completion
- 2020-01-08
- First posted
- 2017-08-03
- Last updated
- 2021-01-05
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT03238742. Inclusion in this directory is not an endorsement.