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Early transfusIon of Convalescent Plasma in Elderly COVID-19 Patients. to Prevent Disease Progression. (LIFESAVER)

Primary Purpose

Coronavirus Disease 2019 )COVID-19)

Status
Completed
Phase
Phase 2
Locations
Italy
Study Type
Interventional
Intervention
COVID-19 Convalescent Plasma
Sponsored by
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Coronavirus Disease 2019 )COVID-19)

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 65
  • pneumonia at CT scan
  • PaO2/FiO2 ≥300 mmHg
  • Presence of one or more comorbidities (consider the list provided in Appendix A)
  • Signed informed consent

Exclusion Criteria:

  • Age < 65
  • PaO2/FiO2 < 300 mmHg
  • pending cardiopulmonary arrest
  • refusal to blood product transfusions
  • Severe IgA deficiency
  • any life-threatening comorbidity or any other medical condition which, in the opinion of the investigator, makes the patient unsuitable for inclusion

Sites / Locations

  • Fondazione Policlinico Universitario A. Gemelli IRCCS
  • Ospedale SS Annunziata
  • Istituto Nazionale Malattie Infettive Lazzaro Spallanzani

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Convalescent plasma

Standard therapy

Arm Description

Patients receive COVID-19 Convalescent Plasma (CCP) in addition to standard therapy

Patients receive standard therapy alone

Outcomes

Primary Outcome Measures

Rate of COVID-19 progression
Proportion of patients without progression in severity of pulmonary disease defined as worsening of 2 points in the ordinal scale of WHO within day 14

Secondary Outcome Measures

Full Information

First Posted
May 2, 2020
Last Updated
May 27, 2021
Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
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1. Study Identification

Unique Protocol Identification Number
NCT04374526
Brief Title
Early transfusIon of Convalescent Plasma in Elderly COVID-19 Patients. to Prevent Disease Progression.
Acronym
LIFESAVER
Official Title
Early transfusIon of COVID-19 Convalescent Plasma in Elderly COVID-19 Patients to Prevent Disease Progression.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
May 27, 2020 (Actual)
Primary Completion Date
May 26, 2021 (Actual)
Study Completion Date
May 26, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fondazione Policlinico Universitario Agostino Gemelli IRCCS

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Older age is an independent poor outcome predictor among COVID-19 hospitalized patients . Among 72,314 COVID-19 cases, case fatality rate (CFR) was 2.3% in total population, 8% in people aged 70 to 79, and 14.8% in those aged 80 and older. In the whole population, CFR was higher in people with comorbidities, ranging from 5-6% in persons with hypertension, chronic respiratory disease, diabetes or cancer, up to 10% in those with cardiovascular diseases. Sars-CoV-2 seems to be able to induce a functional exhaustion of specified T and NK lymphocyte subpopulations, breaking down antiviral immunity. One possible explanation is that the immune system of elderly people, might be exhausted by chronic stimulation associated with comorbidities and more susceptible to this Sars-CoV-2 effect. As a result, in these patients, the activation of the innate immune system might fail to produce an adequate adaptive response (i.e., virus-specific CD8+ T-cells). This results in persistent self-induced inflammation that eventually causes mortality. The investigators hypothesize that transfusing convalescent plasma (containing neutralizing antibodies) at an early phase of COVID-19 infection could prevent or switch off the persistent inflammatory response elicited by the virus. The objective of this study are: To demonstrate the superiority of COVID-19 convalescent plasma (CCP) plus standard therapy (ST) over ST alone To prevent progression of pneumonia in COVID-19 patients aged ≥65 with chronic comorbidities To decrease viral load To raise anti-SARS-CoV-2 antibody titer in recipients

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronavirus Disease 2019 )COVID-19)

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
29 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Convalescent plasma
Arm Type
Experimental
Arm Description
Patients receive COVID-19 Convalescent Plasma (CCP) in addition to standard therapy
Arm Title
Standard therapy
Arm Type
No Intervention
Arm Description
Patients receive standard therapy alone
Intervention Type
Biological
Intervention Name(s)
COVID-19 Convalescent Plasma
Other Intervention Name(s)
CCP
Intervention Description
ABO matched pathogen-inactivated CCP is transfused at a dose of 200 ml/day for 3 days (days 1, 2, and 3).
Primary Outcome Measure Information:
Title
Rate of COVID-19 progression
Description
Proportion of patients without progression in severity of pulmonary disease defined as worsening of 2 points in the ordinal scale of WHO within day 14
Time Frame
days 1 to 14.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 65 pneumonia at CT scan PaO2/FiO2 ≥300 mmHg Presence of one or more comorbidities (consider the list provided in Appendix A) Signed informed consent Exclusion Criteria: Age < 65 PaO2/FiO2 < 300 mmHg pending cardiopulmonary arrest refusal to blood product transfusions Severe IgA deficiency any life-threatening comorbidity or any other medical condition which, in the opinion of the investigator, makes the patient unsuitable for inclusion
Facility Information:
Facility Name
Fondazione Policlinico Universitario A. Gemelli IRCCS
City
Roma
State/Province
RM
ZIP/Postal Code
00168
Country
Italy
Facility Name
Ospedale SS Annunziata
City
Chieti
ZIP/Postal Code
66100
Country
Italy
Facility Name
Istituto Nazionale Malattie Infettive Lazzaro Spallanzani
City
Rome
ZIP/Postal Code
00149
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
33092632
Citation
Teofili L, Landolfi R, Cingolani A, Antinori A, Vecchiet J, Sanguinetti M, Gasbarrini A, Pasciuto T, Orlando N, Lamonica S. "Early transfusion of convalescent plasma in older patients with COVID-19 to prevent disease progression: A structured summary of a study protocol for a randomised controlled trial". Trials. 2020 Oct 22;21(1):875. doi: 10.1186/s13063-020-04821-1.
Results Reference
derived

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Early transfusIon of Convalescent Plasma in Elderly COVID-19 Patients. to Prevent Disease Progression.

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