COVID-19 With Convalescent Plasma
Completed
- Conditions
- COVID-19 Convalescent Plasma Treatment
- Interventions
- Biological: convalescent plasma
- Registration Number
- NCT04616976
- Lead Sponsor
- Southeast University, China
- Brief Summary
To clarify the effects of convalescent plasma therapy on SARS-CoV-2 negative conversion rate during hospital stay and 28-day mortality of severe and life-threatening COVID-19 patients.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 78
Inclusion Criteria
- > 18 years of age;
- laboratory-confirmed diagnosis of COVID-19;
- respiratory failure requiring advanced respiratory support (i.e. high flow nasal cannula[HFNC], noninvasive mechanical ventilation [NIV], and invasive mechanical ventilation [IMV]).
Exclusion Criteria
- no
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description convalescent plasma therapy group convalescent plasma the patients received convalescent plasma therapy
- Primary Outcome Measures
Name Time Method 28-day mortality 28 days the mortality from ICU admission to 28 days after admission
- Secondary Outcome Measures
Name Time Method SARS-CoV-2 negative conversion rate up to 60 days SARS-CoV-2 viral shedding
Trial Locations
- Locations (1)
Zhongda Hospital, Southeast University
🇨🇳Nanjing, Jiangsu, China