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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05269888
Other study ID # 3200
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date February 16, 2022
Est. completion date December 30, 2024

Study information

Verified date July 2023
Source University Hospitals of North Midlands NHS Trust
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Coronavirus (Covid-19) has affected millions of people worldwide. Vaccines to prevent Covid-19 infection have been offered to reduce the risk of infection. While these vaccines have been offered to people with multiple sclerosis (MS), they have not been tested in these individuals. It is uncertain whether people with MS will develop protective antibodies after a Covid-19 vaccination and how long these antibodies will last. The investigators are planning to study the immune response to the full course of Covid-19 vaccine in people with MS (study group) and compare this to people without MS or immune suppression (control group).


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 240
Est. completion date December 30, 2024
Est. primary completion date December 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria (Study Group - MS Patients): - Aged 18 years and over - Diagnosis of Multiple Sclerosis as per McDonald's Criteria 2017 - Falls into one of following the Disease Modification Treatment (DMT) groups: on Ocrelizumab, on Natalizumab, on Alemtuzumab, on Tecfidera, on Fingolimod, on Interferon, not on any DMT - Has had a complete course of Covid-19 vaccination including any boosters (standard dosing: prescribed as per the UK Government guidelines) - Willing and able to give fully informed consent - Willing and able to comply with the study procedures Exclusion Criteria (Study Group - MS Patients): - Has declined or does not wish to have Covid-19 vaccine - Has switched DMT since the date of first dose of Covid-19 vaccine - Has any other immunological condition or on immune treatment causing immune suppression - Has declined or does not wish to have Covid-19 vaccine - Ineligible* for Covid-19 vaccine (*Ineligible for health reasons and/or as per Government prioritisation of vaccinations) - Non-English speaker where translation facilities are insufficient to guarantee informed consent Inclusion Criteria (Control Group - Healthy Volunteers): - Aged 18 years and over - Has had a complete course of Covid-19 vaccination (standard dosing: prescribed as per the UK Government guidelines) - Willing and able to give fully informed consent - Willing and able to comply with the study procedures Exclusion Criteria (Control Group - Healthy Volunteers): - Has declined or does not wish to have Covid-19 vaccine - Has MS or another long-term immunological condition - History of taking any immune treatment causing immune suppression in the last 5 years - History of any immune conditions or comorbidities known to result in immune suppression within the last 5 years; - Ineligible* for Covid-19 vaccine (*Ineligible for health reasons and/or as per Government prioritisation of vaccinations) - Currently participating in one or more interventional trials involving immune suppression or immune agent - Non-English speaker where translation facilities are insufficient to guarantee informed consent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Blood Test 1
Blood test 1 - At 12 months (+3months) from the date of 1st Covid-19 vaccine: Anti-SARS-CoV-2 S1/S2/N IgG antibody Roche, T-SPOT® COVID SARS-CoV-2, Full Blood Count, Serum Immunoglobulins, Anti-VZV titres
Blood Test 2
Blood test 2 - At 18 months (+3months) from the date of 1st Covid-19 vaccine: Anti-SARS-CoV-2 S1/S2/N IgG antibody Roche, T-SPOT® COVID SARS-CoV-2, Full Blood Count, Serum Immunoglobulins, Anti-VZV titres

Locations

Country Name City State
United Kingdom University Hospitals of North Midlands NHS Trust Stoke-on-Trent

Sponsors (1)

Lead Sponsor Collaborator
University Hospitals of North Midlands NHS Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood titres of Anti-SARS-CoV-2 S1/S2/N IgG antibody Roche in MS patients compared with healthy volunteers 12 months from date of first dose of Covid-19 vaccine Anti-SARS-CoV-2 S1/S2/N IgG antibody Roche 12 months (+3 months) from date of first dose of Covid-19 vaccine
Primary Blood titres of Anti-SARS-CoV-2 S1/S2/N IgG antibody Roche in MS patients compared with healthy volunteers 18 months from date of first dose of Covid-19 vaccine Anti-SARS-CoV-2 S1/S2/N IgG antibody Roche 18 months (+3 months) from date of first dose of Covid-19 vaccine
Primary T-SPOT® COVID SARS-CoV-2 test status in MS patients compared with healthy volunteers 12 months from date of first dose of Covid-19 vaccine T-SPOTĀ® COVID SARS-CoV-2 test status 12 months (+3 months) from date of first dose of Covid-19 vaccine
Primary T-SPOT® COVID SARS-CoV-2 test status in MS patients compared with healthy volunteers 18 months from date of first dose of Covid-19 vaccine T-SPOTĀ® COVID SARS-CoV-2 test status 18 months (+3 months) from date of first dose of Covid-19 vaccine
Secondary Type and timing of DMT in MS patients Type and timing of DMT 12 months (+3 months) from date of first dose of Covid-19 vaccine
Secondary Type and timing of DMT in MS patients Type and timing of DMT 18 months (+3 months) from date of first dose of Covid-19 vaccine
Secondary Type and timing of Covid-19 vaccine in MS patients compared with healthy volunteers Type and timing of Covid-19 vaccine 12 months (+3 months) from date of first dose of Covid-19 vaccine
Secondary Type and timing of Covid-19 vaccine in MS patients compared with healthy volunteers Type and timing of Covid-19 vaccine 18 months (+3 months) from date of first dose of Covid-19 vaccine
Secondary Participant-reported PCR positive Covid-19 infection/s in MS patients compared with healthy volunteers Participant-reported PCR positive Covid-19 infection/s 12 months (+3 months) from date of first dose of Covid-19 vaccine
Secondary Participant-reported PCR positive Covid-19 infection/s in MS patients compared with healthy volunteers Participant-reported PCR positive Covid-19 infection/s 18 months (+3 months) from date of first dose of Covid-19 vaccine
Secondary Covid-19 vaccine-related serious adverse events in MS patients compared with healthy volunteers Vaccine-related serious adverse events 12 months (+3 months) from date of first dose of Covid-19 vaccine
Secondary Covid-19 vaccine-related serious adverse events in MS patients compared with healthy volunteers Vaccine-related serious adverse events 18 months (+3 months) from date of first dose of Covid-19 vaccine
Secondary Demographics of MS patients compared with healthy volunteers Demographics 12 months (+3 months) from date of first dose of Covid-19 vaccine
Secondary Demographics of MS patients compared with healthy volunteers Demographics 18 months (+3 months) from date of first dose of Covid-19 vaccine
Secondary Co-morbidity status of MS patients compared with healthy volunteers Co-morbidity status 12 months (+3 months) from date of first dose of Covid-19 vaccine
Secondary Co-morbidity status of MS patients compared with healthy volunteers Co-morbidity status 18 months (+3 months) from date of first dose of Covid-19 vaccine
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