The COVID-19 PUI Reality Check (CPRC) Study

NCT ID: NCT04474288

Last Updated: 2022-03-11

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 37 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2020-07-16
• Study Completion Date: 2022-02-28

Brief Summary

This study compares SARS-CoV-2 immune responses in high pretest probability swab negative hospitalized PUI patients vs. low pretest probability swab negative hospitalized APS (Asymptomatic Persons being Screened) patients to try to understand the appropriateness and safety of clinical decisions made in these patient populations based on swab results.

Detailed Description

This is essentially a two phase blood drawing and immune assays study. Phase 1 will be a single convalescent timing immune retrospective study; phase 2 will include paired samples to increase immune response accuracy in a prospective study. In phase 1, hospitalized PUI and APS patients with negative nasopharyngeal PCR swabs selected by Epic query of Bassett records, will be contacted by telephone (or in person if hospitalized), offered enrollment in the study, and provided informed consent if they're interested. For consented/enrolled patients, routine baseline demographic and clinical data will be obtained by interview (in person or telephone) and/or EMR (Epic) review. These data will be needed to describe baseline characteristics and to assess for predictors of serologic conversion and other immune responses in the two study populations. Up to two to three visits will be required for brief interviews, record review, and blood draws. Phase 1 patients will have visits/blood draws on days 14 and 28 after hospitalization or at 28 days after hospitalization only (-3 days, +60 days) if patients are beyond day 14 at the time of study initiation; phase 2 patients will have visits/blood draws aiming for days 0, 14 (+/- 3 days), and 28 (+/- 3 days) after hospital admission.

Blood will be drawn for SARS-CoV-2 specific immune assays (below). For phase 1 patients, baseline immune assays will not be available as blood is not available for them; thus, for many phase 1 patients, only one of the day 14 and 28 immune assays will be practical. In Phase 2, these procedures will be the same except baseline blood draws will be possible at hospitalization as well. Thus, blood drawing will be at target days 0, 14, and 28 for phase 2 patients. Short interviews at days 14 and 28 will be conducted to assess for new COVID-19 compatible illnesses that may confound immune response results.

Up to 27.5 ml of blood will be required at each timepoint (PAXgene tube 2.5 ml, heparinized tube 10 ml, EDTA tube 10 ml, SST tube 5 ml). Total blood drawing will be up to 55 ml in phase 1 patients and up to 82.5 ml in phase 2 patients. Serologic and additional immune assays will be conducted on blood drawn at these time points to assess for SARS-CoV-2 specific immune responses (see below).

Conditions

Covid19 Immunology

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: OTHER

Study Groups

Person Under Investigation (PUI)

PUI's are subjects who were admitted to the hospital with symptoms suspicious for COVID-19.

SARS-CoV-2 antibody testing

Intervention Type: DIAGNOSTIC_TEST

venipuncture for SARS-CoV-2 IgG

Asymptomatic Person under Screening (APS)

APS's are those patients who do NOT meet the criteria to be a suspect COVID- 19 patient but are being tested because they are being admitted, are required for testing by state mandate, or are having a procedure, etc.

SARS-CoV-2 antibody testing

Intervention Type: DIAGNOSTIC_TEST

venipuncture for SARS-CoV-2 IgG

Interventions

SARS-CoV-2 antibody testing

venipuncture for SARS-CoV-2 IgG

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

Inclusion Criteria

• Hospitalized patient (PUI or APS) and tested for SARS-CoV-2 by NP PCR swab
• At least one negative SARS-CoV-2 NP PCR swab within 2 wks of hospitalization
• Adult >/= 18 yrs old
• Patient or LAR provides informed consent
• Patient or LAR agree to follow-up procedures in informed consent form

Exclusion Criteria

• Prior reaction to blood drawing considered significant safety issue by study investigator
• Other factor considered significant safety issue by study investigator
• At least one positive SARS-CoV-2 NP PCR swab within 2 wks of hospitalization

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Bioreference, Inc

UNKNOWN

Sponsor Role: collaborator

Bassett Healthcare

OTHER

Sponsor Role: lead

Responsible Party

Daniel Freilich, MD

attending physician - hospitalist/infectious disease

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Daniel Freilich, MD

Role: PRINCIPAL_INVESTIGATOR

Bassett Medical Center

Locations

Bassett Medical Center

Cooperstown, New York, United States

Countries

United States

Other Identifiers

1613182

Identifier Type: -

Identifier Source: org_study_id