Anti-SARS-CoV-2 Infection, SARS-CoV-2 Infection
Conditions
Keywords
Immunoglobulin G, Immunoglobulin M
Brief summary
This is a multi-center, prospective registry study of subjects undergoing hemodialysis for treatment of end-stage renal disease in a DaVita center. The objective of this study is to understand whether and to what degree anti-SARS-CoV-2 antibodies mitigate the risk of subsequent SARS-CoV-2 infection and COVID disease within the ESKD population.
Detailed description
This is a multi-center, prospective registry study of subjects undergoing hemodialysis for treatment of end-stage renal disease in a DaVita center. The objective of this study is to understand whether and to what degree anti-SARS-CoV-2 antibodies mitigate the risk of subsequent SARS-CoV-2 infection and COVID disease within the ESKD population. Following informed consent, participants will undergo baseline serologic characterization for anti-SARS-CoV-2 IgM and IgG. The study is planned to align with the present wave of COVID-19. Enrollment will continue until the total sample size of 2500 is reached or until the study sponsor determines. Should there be a subsequent wave of COVID- 19, participants will be actively surveiled for evidence of SARS-CoV-2 infection and for COVID-19 disease. The relationship between baseline serologic status and subsequent infection/disease will be determined. This study will have 2 distinct phases. Phase 1 (baseline characterization) start will be triggered by the sponsor and may start at different times at the active sites. Participants will be consented and enrolled and blood will be collected for anti-SARS-CoV-2 antibodies. Phase 2: Start will be triggered by the sponsor in the fall of 2020 and each geographic study location may be triggered to start at separate times. Study participants will be followed prospectively for incidence and severity of COVID-19. Study visits will commence upon sponsor trigger and will occur once monthly for 4 months.
Interventions
None listed
Sponsors
Davita Clinical Research
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Between ≥18 and 80 years of age, inclusive. * Ability to provide informed consent. * Currently receiving hemodialysis treatment for end-stage kidney disease at a DaVita dialysis center.
Exclusion criteria
\-
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Anti-SARS-CoV-2 antibodies | Through study completion (5 visits), an average of 6 months |
| Incidence and severity of COVID-19 | Through study completion (5 visits), an average of 6 months |
Countries
United States
Outcome results
None listed