Multiple Sclerosis Clinical Trial
Official title:
DECISIve - DiagnosE Using the Central veIn SIgn. A Prospective Diagnostic Superiority Study Comparing T2* MRI and Lumbar Puncture in Patients Presenting With Possible Multiple Sclerosis
There is currently no agreement on the best way to diagnose Multiple Sclerosis (MS).
Frequently, people suspected of having MS have a standard MRI scan and undergo a 'lumbar
puncture' (a thin needle is inserted between the bones in the lower spine). Patients often
report they find it painful and it can cause unintended complications requiring
hospitalisations or time off work to recover.
Although the fluid taken during a lumbar puncture can show evidence of disease, this is not
always the case. Doctors do not find abnormalities in everyone who has MS but some people
with conditions that can mimic MS, but need very different treatment, have similar lumbar
puncture abnormalities. Both of these problems can lead to misdiagnosis.
A new MRI scan allows doctors to see small veins that run through damaged areas of the brain
in people with MS. It has been shown that this is a specific finding to MS, seldom seen in
other conditions. It is not painful and carries few or no risks.
This research aims to change the way people are diagnosed with MS and reduce the number of
lumbar punctures used. The investigators will recruit a large number of people from different
hospitals whose doctors suspect they may have MS. They will be invited to have the new
eight-minute MRI scan. After 18 months, the investigators will find out what diagnosis is
eventually reached and compare this to the finding of the new scan. The investigators will
then compare the accuracy, speed, costs and acceptability of the different tests needed to
make a diagnosis of MS and establish if most lumbar punctures can be replaced by a slightly
longer MRI scan. This research could provide the National Health Service with a scientific
approach to diagnose MS which is safer, more cost effective and importantly, more acceptable
to patients.
The North American Imaging in MS Cooperative has reviewed the utility of the central vein
sign (CVS) in the diagnosis of MS in 2015. They concluded that "To formally establish the
clinical value of the CVS for the differential diagnosis at disease onset, a large,
prospective, multicentre study including patients at first presentation of possible MS is
necessary". The paper outlining the 2017 McDonald diagnostic criteria for MS specifically
mentions the promise of the CVS but suggests that it "requires detailed investigation to
determine whether it is useful and practical". The rationale of this study is to provide an
overwhelming case for a straightforward and rapid clinical adoption of our MRI test, which
will change our ability to confirm or refute the diagnosis of MS.
Radiologists and neurologists can also readily interpret our proposed CVS using a simple
'rule of six' that was described in a previous study. This involves the detection of any six
lesions with a central vein present. This rule has the potential to be easily implemented in
clinical practice if it has superior diagnostic sensitivity, when compared to lumbar puncture
results.
If the CVS can be shown to have superior diagnostic sensitivity at first presentation of MS,
when compared to performing a lumbar puncture, then lumbar punctures can be avoided in many
patients. These patients will benefit in several ways. The patients will avoid a procedure
that is often painful or unpleasant. Those who currently refuse to have lumbar puncture will
benefit from expedited diagnosis, limiting their anxiety and uncertainty. A secure diagnosis
could lead to more rapid treatment decisions and a better long-term prognosis. In addition,
fewer workdays will be lost attending hospital for investigation. From the NHS' perspective,
it would avoid day case hospital admissions for lumbar punctures and readmissions to treat
the common complication of post lumbar puncture headaches. This would create significant cost
savings, when considering the significant number of patients undergoing this diagnostic
process.
;
| 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 |