Skip to content

COVID-19 With Convalescent Plasma

Efficiency of Convalescent Plasma Therapy in Management of Critically Ill Patients With COVID-19: a Matched Case-control Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04616976
Enrollment
78
Registered
2020-11-05
Start date
2020-01-01
Completion date
2020-11-01
Last updated
2020-11-05

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

Conditions

COVID-19 Convalescent Plasma Treatment

Keywords

convalescent plasma therapy, COVID-19, mortality

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.

Interventions

BIOLOGICALconvalescent plasma

convalescent plasma was get from the patients who recovery from COVID-19

Sponsors

Southeast University, China
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. \> 18 years of age; 2. laboratory-confirmed diagnosis of COVID-19; 3. 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

Design outcomes

Primary

MeasureTime frameDescription
28-day mortality28 daysthe mortality from ICU admission to 28 days after admission

Secondary

MeasureTime frameDescription
SARS-CoV-2 negative conversion rateup to 60 daysSARS-CoV-2 viral shedding

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026