NYU Langone Health
New York, 10016, United States
NCT Number: NCT04682548
This non-interventional, biospecimen collection study is designed to help us better understand whether MS patients have impaired immune defenses to COVID-19 infection. The potential influence of immune modulating medications for MS will be considered through these exploratory studies. This study is also designed to provide context for interpretation of anti-SARS CoV2 serologies in MS patients during convalescence from COVID-19 infection.
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Notify Me18 year–60 year
All sexes
Observational
New York, 10016, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
(Part A and B):
● Patient is outside of infectious period of COVID-19 defined as follows:
Inclusion criteria
(Part B only)
Inclusion Critera (Redraws Only)
Exclusion criteria
(Part A and B):
Exclusion criteria
(Part B only):
Exclusion criteria
(Healthy Controls Sample)
Time frame: Baseline, Day 0
Seropositivity rate against SARS-CoV-2 (nucleocapsid and/or spike proteins, as available) as measured by the Roche DIA antibody assay in MS patients.
Time frame: Baseline, Day 0
SARS-CoV-2 specific T cells will be measured using a well-validated assay such as ELISpot (enzyme-linked immune absorbent spot) to measure T cell responses to stimulation.
Time frame: Baseline, Day 0
SARS-CoV-2 specific T cells will be measured using a well-validated assay such as ELISpot (enzyme-linked immune absorbent spot) to measure T cell responses to stimulation.
Time frame: up to week 48 Post-Vaccination
SARS-CoV-2 specific T cells will be measured using a well-validated assay such as ELISpot (enzyme-linked immune absorbent spot) to measure T cell responses to stimulation.
Time frame: Baseline, Day 0
SARS-CoV-2 antibodies will be measured and assessed with Roche DIA Assay
Time frame: up to week 48 Post-Vaccination
SARS-CoV-2 antibodies will be measured and assessed with Roche DIA Assay
NYU Langone Health
Other
Estimating Prevalence of COVID-19 Infection and SARS-CoV-2 Antibodies in MS Patients With and Without Ocrelizumab Treatment, and Comparing Immune Responses to COVID-19 in MS Patients on Ocrelizumab and Healthy Controls
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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