Passive Immunity Trial for Our Nation to Treat COVID-19 in Hospitalized Adults
PassItOn
2 other identifiers
interventional
974
1 country
26
Brief Summary
The purpose of this study is to test the safety and efficacy of convalescent donor plasma to treat COVID-19 in hospitalized adults in a randomized, placebo-controlled setting. The effect of convalescent plasma will be compared to placebo on clinical outcomes, measured using the COVID-19 7-point Ordinal Clinical Progression Outcomes Scale at Day 15, among adults with COVID-19 requiring hospitalization.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for phase_3 covid19
Started Apr 2020
Typical duration for phase_3 covid19
26 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 21, 2020
CompletedFirst Posted
Study publicly available on registry
April 24, 2020
CompletedStudy Start
First participant enrolled
April 24, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 6, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
August 6, 2021
CompletedResults Posted
Study results publicly available
November 3, 2022
CompletedNovember 3, 2022
October 1, 2022
1.2 years
April 21, 2020
July 6, 2022
October 6, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
COVID-19 7-point Ordinal Clinical Progression Outcomes Scale Score
Outcome measured clinical status of the participant defined by the Covid-19 7-point Ordinal Clinical Progression Outcomes Scale: This scale reflects a range from baseline to death as follows: 1. Not hospitalized with resumption of normal activities. 2. Not hospitalized, but unable to resume normal activities. 3. Hospitalized, not on supplemental oxygen. 4. Hospitalized, on supplemental oxygen. 5. Hospitalized, on nasal high-flow oxygen therapy, noninvasive mechanical ventilation, or both 6. Hospitalized, on ECMO, invasive mechanical ventilation, or both. 7. Death
Study Day 15
Secondary Outcomes (11)
All-location, All-cause 14-day Mortality
Baseline to Study Day 14
All-location, All-cause 28-day Mortality
Baseline to Study Day 28
Survival Through 28 Days
Baseline to Day 28 (assessed on Study Day 29)
COVID-19 7-point Ordinal Clinical Progression Outcomes Scale on Study Day 3
Baseline to Study Day 3
COVID-19 7-point Ordinal Clinical Progression Outcomes Scale on Study Day 8
Study Day 8
- +6 more secondary outcomes
Other Outcomes (8)
Acute Kidney Injury
Baseline to Day 28
Renal Replacement Therapy
Baseline to Day 28
Documented Venous Thromboembolic Disease (DVT or PE)
Baseline to Day 28
- +5 more other outcomes
Study Arms (2)
pathogen reduced SARS-CoV-2 convalescent plasma
EXPERIMENTALTransfusion of convalescent plasma will be administered by clinical or research personnel while the participant is hospitalized on Study Day 0. Plasma will be administered at a rate of 500 mL/hour and will be administered within 12 hours of randomization.
Placebo
PLACEBO COMPARATORParticipants randomized to the control group will receive 250mL of Lactate Ringers containing multivitamins intravenously on Day 1 as a placebo.
Interventions
Convalescent COVID-19 donor plasma is the liquid part of blood that is collected from patients who have recovered from COVID-19 infection. This plasma contains SARS-CoV-2 specific antibodies that may help fight the infection.
Eligibility Criteria
You may qualify if:
- Age greater than or equal to 18 years
- Currently hospitalized or in an emergency department with anticipated hospitalization
- Symptoms of acute respiratory infection, defined as one or more of the following:
- Cough
- Chills, or a fever (greater than 37.5° C or 99.5° F)
- Shortness of breath, operationalized as a patient having any of the following:
- i. Subjective shortness of breath reported by a patient or surrogate. ii. Tachypnea with respiratory rate of greater than 22 breaths per minute iii. Hypoxemia, defined as SpO2 less than 92% on room air, new receipt of supplemental oxygen to maintain SpO2 greater than or equal to 92%, or increased supplemental oxygen to maintain SpO2 greater than or equal to 92% for a patient on chronic oxygen therapy
- Laboratory-confirmed SARS-CoV-2 infection within the past 14 days
You may not qualify if:
- Prisoner
- Unable to randomize within 14 days after onset of acute respiratory infection symptoms
- Patient, legal representative, or physician not committed to full support (Exception: a patient who will receive all supportive care except for attempts at resuscitation from cardiac arrest will not be excluded.)
- Inability to be contacted on Day 29-36 for clinical outcome assessment
- Receipt of any SARS-CoV-2 passive immunity therapy, such as convalescent plasma, monoclonal antibodies, or pooled immunoglobulin, in the past 30 days
- Contraindications to transfusion or history of prior reactions to transfused blood products
- Plan for hospital discharge within 24 hours of enrollment
- Previous enrollment in this trial
- Previous laboratory-confirmed SARS-CoV-2 infection before the current illness
- Enrollment in another clinical trial evaluating monoclonal antibodies, convalescent plasma, or another passive immunity therapy
- Prior receipt of SARS-CoV-2 vaccine
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Vanderbilt University Medical Centerlead
- Dolly Partoncollaborator
- National Center for Advancing Translational Sciences (NCATS)collaborator
Study Sites (26)
University of Arkansas for Medical Sciences
Little Rock, Arkansas, 72205, United States
Scripps Health
La Jolla, California, 92037, United States
University of Colorado Denver
Aurora, Colorado, 80045, United States
MedStar Health Research Institute/MedStar Washington Hospital Center
Washington D.C., District of Columbia, 20010, United States
Cleveland Clinic Florida
Weston, Florida, 33331, United States
University of Chicago
Chicago, Illinois, 60637, United States
Loyola University Medical Center
Maywood, Illinois, 60153, United States
The University of Kansas Medical Center
Kansas City, Kansas, 66160, United States
Our Lady of the Lake Regional Medical Center
Baton Rouge, Louisiana, 70808, United States
University of Maryland, Baltimore (University of Maryland Medical Center)
Baltimore, Maryland, 21201, United States
Beth Israel Deaconess Medical Center
Boston, Massachusetts, 02215, United States
Newton-Wellelsey Hospital
Newton, Massachusetts, 012462, United States
University of Minnesota
Minneapolis, Minnesota, 55455, United States
University of Mississippi Medical Center
Jackson, Mississippi, 39216, United States
University of New Mexico Health Sciences Center
Albuquerque, New Mexico, 87131, United States
University at Buffalo/Buffalo General Medical Center
Buffalo, New York, 14203, United States
Rochester General Hospital
Rochester, New York, 14621, United States
Cleveland Clinic Ohio
Cleveland, Ohio, 44195, United States
The Ohio State University Wexner Medical Center and James Cancer Hospital
Columbus, Ohio, 43210, United States
Vanderbilt University Medical Center
Nashville, Tennessee, 37203, United States
Meharry Medical College
Nashville, Tennessee, 37208, United States
Utah Valley Hospital
Provo, Utah, 84604, United States
University of Utah Health
Salt Lake City, Utah, 84132, United States
Sentara Norfolk General Hospital
Norfolk, Virginia, 23507, United States
Virginia Commonwealth University
Richmond, Virginia, 23298, United States
University of Washington
Seattle, Washington, 98104, United States
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PMID: 33743799DERIVEDSelf WH, Stewart TG, Wheeler AP, El Atrouni W, Bistran-Hall AJ, Casey JD, Cataldo VD, Chappell JD, Cohn CS, Collins JB, Denison MR, de Wit M, Dixon SL, Duggal A, Edwards TL, Fontaine MJ, Ginde AA, Harkins MS, Harrington T, Harris ES, Hoda D, Ipe TS, Jaiswal SJ, Johnson NJ, Jones AE, Laguio-Vila M, Lindsell CJ, Mallada J, Mammen MJ, Metcalf RA, Middleton EA, Mucha S, O'Neal HR, Pannu SR, Pulley JM, Qiao X, Raval JS, Rhoads JP, Schrager H, Shanholtz C, Shapiro NI, Schrantz SJ, Thomsen I, Vermillion KK, Bernard GR, Rice TW. Passive Immunity Trial for Our Nation (PassITON): study protocol for a randomized placebo-control clinical trial evaluating COVID-19 convalescent plasma in hospitalized adults. Res Sq [Preprint]. 2021 Mar 2:rs.3.rs-227796. doi: 10.21203/rs.3.rs-227796/v1.
PMID: 33688640DERIVED
Related Links
- Discovery of a novel coronavirus associated with the recent pneumonia outbreak in humans and its potential bat origin
- China puts 245 COVID-19 patients on convalescent plasma therapy - Xinhua
- Elevated Serum IgM Levels Indicate Poor Outcome in Patients with Coronavirus Disease 2019 Pneumonia: A Retrospective Case-Control Study. Rochester, NY: Social Science Research Network
- WHO \| Coronavirus disease (COVID-2019) R\&D
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Results Point of Contact
- Title
- Todd Rice, M.D., MSc
- Organization
- Vanderbilt University Medical Center
Study Officials
- PRINCIPAL INVESTIGATOR
Todd Rice, MD
Vanderbilt University Medical Center
Publication Agreements
- PI is Sponsor Employee
- Yes
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor of Medicine
Study Record Dates
First Submitted
April 21, 2020
First Posted
April 24, 2020
Study Start
April 24, 2020
Primary Completion
July 6, 2021
Study Completion
August 6, 2021
Last Updated
November 3, 2022
Results First Posted
November 3, 2022
Record last verified: 2022-10
Data Sharing
- IPD Sharing
- Will not share