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Convalescent Plasma for Patients With COVID-19: A Pilot Study

Convalescent Plasma for Patients With COVID-19: A Pilot Study

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04332380
Acronym
CP-COVID-19
Enrollment
10
Registered
2020-04-02
Start date
2020-05-01
Completion date
2020-07-28
Last updated
2020-08-17

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

Conditions

Coronavirus, Coronavirus Infection

Keywords

COVID-19, Coronavirus Disease 2019

Brief summary

Convalescent plasma (CP) has been used in recent years as an empirical treatment strategy when there is no vaccine or treatment available for infectious diseases. In the latest viral epidemics, such as the Ebola outbreak in West Africa in 2014, the World Health Organization issued a document outlining a protocol for the use of whole blood or plasma collected from patients who have recovered from the Ebola virus disease by transfusion to empirically treat local infectious outbreaks.

Detailed description

The process is based on obtaining plasma from patients recovered from COVID-19 in Colombia, and through a donation of plasma from the recovered, the subsequent transfusion of this to patients infected with coronavirus disease (COVID-19). Our group has reviewed the scientific evidence regarding the application of convalescent plasma for emergency viral outbreaks and has recommended the following protocol

Interventions

DRUGPlasma

Day 1: CP-COVID19, 250 milliliters. Day 2: CP-COVID19, 250 milliliters.

Sponsors

CES University
CollaboratorOTHER
Instituto Distrital de Ciencia Biotecnologia e Innovacion en salud
CollaboratorUNKNOWN
Fundación Universitaria de Ciencias de la Salud
CollaboratorOTHER
Universidad del Rosario
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Fulfilling all the following criteria 1. Aged between 18 and 60 years, male or female. 2. Hospitalized participants with diagnosis for COVID 19 by Real Time - Polymerase Chain Reaction. 3. Without treatment. 4. Moderate cases according to the official guideline Pneumonia Diagnosis and Treatment Scheme for Novel Coronavirus Infection (Trial Version 6). 5. Confusion, Urea, Respiratory rate, Blood pressure-65 (CURB-65) \>= 2. 6. Sequential Organ Failure Assessment score (SOFA) \< 6. 7. Ability to understand and the willingness to sign a written informed consent document.

Exclusion criteria

1. Female subjects who are pregnant or breastfeeding. 2. Patients with prior allergic reactions to transfusions. 3. Critical ill patients in intensive care units. 4. Patients with surgical procedures in the last 30 days. 5. Patients with active treatment for cancer (Radiotherapy or Chemotherapy). 6. HIV diagnosed patients with viral failure (detectable viral load\> 1000 copies / ml persistent, two consecutive viral load measurements within a 3 month interval, with medication adherence between measurements after at least 6 months of starting a new regimen antiretrovirals). 7. Patients who have suspicion or evidence of coinfections. 8. End-stage chronic kidney disease (Glomerular Filtration Rate \<15 ml / min / 1.73 m2). 9. Child Pugh C stage liver cirrhosis. 10. High cardiac output diseases. 11. Autoimmune diseases or Immunoglobulin A nephropathy. 12. Patients have any condition that in the judgement of the Investigators would make the subject inappropriate for entry into this study.

Design outcomes

Primary

MeasureTime frameDescription
Change in Viral LoadDays 0, 4, 7, 14 and 28Copies of COVID-19 per ml
Change in Immunoglobulin M COVID-19 antibodies TitersDays 0, 4, 7, 14 and 28Immunoglobulin M COVID-19 antibodies
Change in Immunoglobulin G COVID-19 antibodies TitersDays 0, 4, 7, 14 and 28Immunoglobulin G COVID-19 antibodies

Secondary

MeasureTime frameDescription
Requirement of mechanical ventilationDays 7, 14 and 28Proportion of patients with mechanical ventilation (days 7, 14 and 28)
Duration (days) of mechanical ventilationDays 7, 14 and 28Days with mechanical ventilation (days 7, 14 and 28)
Intensive Care Unit AdmissionDays 7, 14 and 28Proportion of patients with Intensive Care Unit Admission requirement (days 7, 14 and 28)
MortalityDays 7, 14 and 28Proportión of death patients at days 7, 14 and 28
Clinical status assessed according to the World Health Organization guidelineDays 7, 14 and 281\. Hospital discharge; 2. Hospitalization, not requiring supplemental oxygen; 3. Hospitalization, requiring supplemental oxygen (but not Noninvasive Ventilation/ HFNC); 4. Intensive care unit/hospitalization, requiring Noninvasive Ventilation/ HFNC therapy; 5. Intensive care unit, requiring extracorporeal membrane oxygenation and/or invasive mechanical ventilation; 6. Death. (days 7, 14 and 28)
Length of Intensive Care Unit stayDays 7, 14 and 28Days of Intensive Care Unit management (days 7, 14 and 28)
Length of hospital stay (days)Days 7, 14 and 28Days of Hospitalization (days 7, 14 and 28)

Countries

Colombia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026