Multiple Sclerosis Clinical Trial
— CoVaR-MSOfficial title:
An Observational Study to Evaluate Immune Response to Covid-19 Vaccines, Infections and Immune Treatments in People With Multiple Sclerosis
Verified date | July 2023 |
Source | University Hospitals of North Midlands NHS Trust |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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).
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 |
Country | Name | City | State |
---|---|---|---|
United Kingdom | University Hospitals of North Midlands NHS Trust | Stoke-on-Trent |
Lead Sponsor | Collaborator |
---|---|
University Hospitals of North Midlands NHS Trust |
United Kingdom,
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 |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05528666 -
Risk Perception in Multiple Sclerosis
|
||
Completed |
NCT03608527 -
Adaptive Plasticity Following Rehabilitation in Multiple Sclerosis
|
N/A | |
Recruiting |
NCT05532943 -
Evaluate the Safety and Efficacy of Allogeneic Umbilical Cord Mesenchymal Stem Cells in Patients With Multiple Sclerosis
|
Phase 1/Phase 2 | |
Completed |
NCT02486640 -
Evaluation of Potential Predictors of Adherence by Investigating a Representative Cohort of Multiple Sclerosis (MS) Patients in Germany Treated With Betaferon
|
||
Completed |
NCT01324232 -
Safety and Efficacy of AVP-923 in the Treatment of Central Neuropathic Pain in Multiple Sclerosis
|
Phase 2 | |
Completed |
NCT04546698 -
5-HT7 Receptor Implication in Inflammatory Mechanisms in Multiple Sclerosis
|
||
Active, not recruiting |
NCT04380220 -
Coagulation/Complement Activation and Cerebral Hypoperfusion in Relapsing-remitting Multiple Sclerosis
|
||
Completed |
NCT02835677 -
Integrating Caregiver Support Into MS Care
|
N/A | |
Completed |
NCT03686826 -
Feasibility and Reliability of Multimodal Evoked Potentials
|
||
Recruiting |
NCT05964829 -
Impact of the Cionic Neural Sleeve on Mobility in Multiple Sclerosis
|
N/A | |
Withdrawn |
NCT06021561 -
Orofacial Pain in Multiple Sclerosis
|
||
Completed |
NCT03653585 -
Cortical Lesions in Patients With Multiple Sclerosis
|
||
Recruiting |
NCT04798651 -
Pathogenicity of B and CD4 T Cell Subsets in Multiple Sclerosis
|
N/A | |
Active, not recruiting |
NCT05054140 -
Study to Evaluate Efficacy, Safety, and Tolerability of IMU-838 in Patients With Progressive Multiple Sclerosis
|
Phase 2 | |
Completed |
NCT05447143 -
Effect of Home Exercise Program on Various Parameters in Patients With Multiple Sclerosis
|
N/A | |
Recruiting |
NCT06195644 -
Effect of Galvanic Vestibular Stimulation on Cortical Excitability and Hand Dexterity in Multiple Sclerosis Patients
|
Phase 1 | |
Completed |
NCT04147052 -
iSLEEPms: An Internet-Delivered Intervention for Sleep Disturbance in Multiple Sclerosis
|
N/A | |
Completed |
NCT03591809 -
Combined Exercise Training in Patients With Multiple Sclerosis
|
N/A | |
Completed |
NCT03594357 -
Cognitive Functions in Patients With Multiple Sclerosis
|
||
Completed |
NCT03269175 -
BENEFIT 15 Long-term Follow-up Study of the BENEFIT and BENEFIT Follow-up Studies
|
Phase 4 |