CP-COVID-19: Convalescent Plasma for Patients With COVID-19: A Randomized, Single Blinded, Parallel, Controlled Clinical Study

Sponsor
Universidad del Rosario (Other)
Overall Status
Completed
CT.gov ID
NCT04332835
Collaborator
Fundación Universitaria de Ciencias de la Salud (Other), CES University (Other), Instituto Distrital de Ciencia Biotecnología e Innovacion en Salud (Other)
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Study Details

Study Description

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

Condition or Disease Intervention/Treatment Phase
Phase 2/Phase 3

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

Study Design

Study Type:
Interventional
Actual Enrollment :
92 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
Single Blinded
Primary Purpose:
Treatment
Official Title:
Convalescent Plasma for Patients With COVID-19: A Randomized, Single Blinded, Parallel, Controlled Clinical Study
Actual Study Start Date :
Aug 8, 2020
Actual Primary Completion Date :
Oct 31, 2020
Actual Study Completion Date :
Nov 15, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Group

Participants included in the experimental group will receive 500 milliliters of convalescent plasma, distributed in two 250 milliliters transfusions on the first and second day after starting the protocol. Simultaneously, they will receive the standard therapy defined by institutional protocol.

Drug: Plasma
Day 1: CP-COVID19, 250 milliliters. Day 2: CP-COVID19, 250 milliliters.
Other Names:
  • Convalescent Plasma COVID-19
  • Drug: Standard Therapy
    Standard therapy defined by institutional protocol.

    Active Comparator: Control Group

    Participants included in the control group will receive standard therapy defined by institutional protocol.

    Drug: Standard Therapy
    Standard therapy defined by institutional protocol.

    Outcome Measures

    Primary Outcome Measures

    1. Change in Viral Load [Days 0, 4, 7, 14 and 28]

      Copies of COVID-19 per ml

    2. Change in Immunoglobulin G COVID-19 Titers [Days 0, 4, 7, 14 and 28]

      Immunoglobulin G COVID-19 antibodies

    Secondary Outcome Measures

    1. Intensive Care Unit Admission [Days 7, 14 and 28]

      Proportion of patients with Intensive Care Unit Admission requirement (days 7, 14 and 28)

    2. Length of Intensive Care Unit stay [Days 7, 14 and 28]

      Days of Intensive Care Unit management (days 7, 14 and 28)

    3. Length of hospital stay (days) [Days 7, 14 and 28]

      Days of Hospitalization (days 7, 14 and 28)

    4. Requirement of mechanical ventilation [Days 7, 14 and 28]

      Proportion of patients with mechanical ventilation (days 7, 14 and 28)

    5. Duration (days) of mechanical ventilation [Days 7, 14 and 28]

      Days with mechanical ventilation (days 7, 14 and 28)

    6. Clinical status assessed according to the World Health Organization guideline [Days 7, 14 and 28]

      1. 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)

    7. Mortality [Days 7, 14 and 28]

      Proportion of death patients at days 7, 14 and 28

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 100 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Inclusion Criteria:Fulfilling all the following criteria

    1. Olerder than 18.

    2. Hospitalized participants with diagnosis of COVID 19 by Real Time - Polymerase Chain Reaction.

    3. Severe cases according to the official guideline "Pneumonia Diagnosis and Treatment Scheme for Novel Coronavirus Infection (Trial Version 7)".

    4. Sequential Organ Failure Assessment score (SOFA) < 6.

    5. 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 with requierment of Invasive Mechanical Venitlation.

    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. Demonstrated coinfection that explains the patient's symptoms

    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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Universidad del Rosario Bogota Cundinamarca Colombia 11100

    Sponsors and Collaborators

    • Universidad del Rosario
    • Fundación Universitaria de Ciencias de la Salud
    • CES University
    • Instituto Distrital de Ciencia Biotecnología e Innovacion en Salud

    Investigators

    • Study Director: Juan M Anaya Cabrera, MD, PhD, Universidad del Rosario

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Juan Manuel Anaya Cabrera, MD, PhD, Principal Investigator, Universidad del Rosario
    ClinicalTrials.gov Identifier:
    NCT04332835
    Other Study ID Numbers:
    • ABN011-2
    First Posted:
    Apr 3, 2020
    Last Update Posted:
    Nov 27, 2020
    Last Verified:
    Nov 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Juan Manuel Anaya Cabrera, MD, PhD, Principal Investigator, Universidad del Rosario
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 27, 2020