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Cancelled, due to modify the protocol A single-center, open-label and single arm trial to evaluate the efficacy and safety of anti-SARS-CoV-2 inactivated convalescent plasma in the treatment&

A single-center, open-label and single arm trial to evaluate the efficacy and safety of anti-SARS-CoV-2 inactivated convalescent plasma in the treatment of novel coronavirus pneumonia (COVID-19) patient

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030312
Enrollment
Unknown
Registered
2020-02-28
Start date
2020-02-29
Completion date
Unknown
Last updated
2020-03-09

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

Conditions

Novel Coronavirus Pneumonia (COVID-19)

Interventions

Case series:Anti-SARS-CoV-2 virus inactivated plasma

Sponsors

First people's hospital of Jiangxi district,Wuhan
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70 years old; 2. Patients with pneumonia infected by new coronavirus: confirmed cases in compliance with the Diagnosis and Treatment Plan for Pneumonia Infected by New Coronavirus (Sixth Edition); 3. Confirmed cases who can be transfused into anti-SARS-CoV-2 virus inactivated plasma after fully assessing patients condition; 4. Cases who score 3 or 4 according to 6-grade scale; 5. The subjects and/or their legal guardians voluntarily participated in the study and voluntarily signed an informed consent form.

Exclusion criteria

Exclusion criteria: 1. The clinical classification of patients with severe novel coronavirus infection is to meet any of the following: 1) Respiratory failure occurs and requires mechanical ventilation; 2) Shock occurs; 3) Combined failure of other organs requires ICU monitoring and treatment; 2. Those who are allergic to blood products or plasma components and auxiliary materials (sodium citrate); 3. There is multiple organ failure, and the estimated survival time is less than 3 days; 4. Those who tested positive for HIV antibodies before enrollment; 5. Women who are pregnant or breastfeeding or have a birth plan within the past year; 6. Participants in other clinical trials within 3 months before screening; 7.Poor adherence or other conditions that the investigator believes are not suitable for inclusion (such as poor physical condition).

Design outcomes

Primary

MeasureTime frame
Clinical symptom improvement rate: improvement rate of clinical symptoms = number of cases with clinical symptom improvement /number of enrolling cases * 100%;

Secondary

MeasureTime frame
The fading and obviously improving time of clinical symptoms (fever, dry cough, fatigue, etc);The negative conversion rate of new coronavirus nucleic acid;Negative conversion time of new coronavirus nucleic acid;;Time of body temperature normalization;;Time of discharge;;Antibody levels of new coronavirus ;Adverse reactions of plasma infusion;Grade 3 and Grade 4 adverse events;Serious adverse events;

Countries

China

Contacts

Public ContactBende Liu

First People's Hospital of Jiangxi District

liubende99@outlook.com+86 13907191851

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026