CClinicalTrials.gg
Status unknownNCT04292340Updated Mar 3, 2020

Anti-SARS-CoV-2 Inactivated Convalescent Plasma in the Treatment of COVID-19

An observational study in Coronavirus, sponsored by Shanghai Public Health Clinical Center. Status unknown at 1 site in China. Per ClinicalTrials.gov, last updated 2020-03-03.

Sponsored by Shanghai Public Health Clinical Center · Observational

The sponsor has not verified this record recently (last verified Feb 2020), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
15
Sex
All
01

Study summary

There is still no effective antiviral drugs and vaccines against SARS-CoV-2 yet now. This is an obsevational study, the investigators collected the clinical information and clinical outcomes of the COVID-19 patients using anti-2019-nCoV inactivated convalescent plasma.The study is to evaluate the efficacy and safety of anti-2019-nCoV inactivated convalescent plasma in the treatment of COVID-19 pneumonia.

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Conditions studied

  • Coronavirus

Keywords

  • Plasma transfusion
  • Coronavirus
03

In context

Coronavirus Infections

929 studies on the registry are indexed under Coronavirus Infections; 50 are open to participants now.

This study's planned enrollment of 15 is below the median of 300 across 334 observational studies indexed under Coronavirus Infections.

Browse Coronavirus Infections studies →

Lead sponsor

Shanghai Public Health Clinical Center is the lead sponsor of 37 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Participants received anti-SARS-CoV-2 inactivated convalescent plasma

Inclusion criteria

  • The participants were diagnosed as COVID-19;
  • Participants received anti-SARS-CoV-2 inactivated convalescent plasma
  • Written the informed consent.

Exclusion criteria

Exclusion Criteria:

  • Participants lacked detailed medical history
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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
15 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. The virological clearance rate of throat swabs, sputum, or lower respiratory tract secretions at day 1

    The SARS-CoV-2 nuclei acid was quantified using RT-PCR

    Time frame: 1 day after receiving plasma transmission

  2. The virological clearance rate of throat swabs, sputum, or lower respiratory tract secretions at day 3

    Time frame: 3 days after receiving plasma transmission

  3. The virological clearance rate of throat swabs, sputum, or lower respiratory tract secretions at day 7

    Time frame: 7 days after receiving plasma transmission

  4. Numbers of participants with different Clinical outcomes

    Clinical outcomes include death, critical illness, recovery

    Time frame: From receiving plasma transmission to 4 weeks

Secondary outcomes

  1. Number of participants with treatment-related adverse events as assessed by CTCAE v5.0

    Time frame: 4 weeks after receiving plasma transmission

07

Study locations

1 of 1 sites recruiting
  • Shanghai Public Health Clinical Center
    Shanghai, Shanghai 201508, China
    • Jun Chen · Contact · 008602137990333
    Recruiting
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 3, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04292340
Lead sponsor
Shanghai Public Health Clinical Center
Responsible party
Hongzhou Lu (professor, Shanghai Public Health Clinical Center) — Principal investigator
First posted
Mar 3, 2020
Start date
Feb 1, 2020
Primary completion
Jul 31, 2020 (estimated)
Completion
Dec 31, 2020 (estimated)
Last update
Mar 3, 2020

Study contacts

Hongzhou Lu, Ph.D
Contact
luhongzhou@fudan.edu.cn
+86-021-37990333 ext. 3222
Hongzhou Lu, Ph.D
principal investigator · Shanghai Public Health Clinical Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Feb 2020. You cannot join it, but the record below documents what was studied.

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