Multiple Sclerosis Clinical Trial
— DECISiVEOfficial 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.
NCT number | NCT05533905 |
Other study ID # | 19NS022 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | December 9, 2019 |
Est. completion date | November 6, 2023 |
Verified date | March 2024 |
Source | Nottingham University Hospitals NHS Trust |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
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
Status | Completed |
Enrollment | 113 |
Est. completion date | November 6, 2023 |
Est. primary completion date | November 6, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: - Presentation with a typical clinically isolated syndrome (Thompson et al. 2017) for diagnostic evaluation of MS. Exclusion Criteria: 1. Fulfils the diagnosis of MS, as defined by the 2017 revision of McDonald diagnostic criteria (Thompson et al. 2017). 2. Unwilling or unable to comply with the requirements of this protocol including the presence of any condition (physical, mental, or social) that, in the opinion of the PI, is likely to affect the participant's ability to comply with the study protocol. 3. Unable to provide informed consent. 4. Contraindication or inability to undergo MRI due to metal or metal implants, pregnancy, claustrophobia, pain, spasticity, or excessive movement related to tremor. 5. Acute COVID-19 infection at time of face-to-face interactions during study (unless investigations can be delayed until considered safe by the responsible clinician and PI) either diagnosed clinically or by acute infection testing 6. Participant required to self-isolate at time of face-to-face interactions during study (unless investigations can be delayed until considered safe by the responsible clinician and PI) due to COVID-19 exposure, shielding due to medical advice, public health advice or governmental advice/laws. |
Country | Name | City | State |
---|---|---|---|
United Kingdom | NUH NHS Trust | Nottingham |
Lead Sponsor | Collaborator |
---|---|
Nottingham University Hospitals NHS Trust |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Is T2* MRI scan more sensitive than lumbar puncture with oligoclonal band testing for diagnosing MS at the time of first clinical presentation? | Comparison of MRI and lumbar puncture in diagnosing MS. | 18 months | |
Secondary | Is there a significant difference between the specificity of each diagnostic test in this cohort? | Is there a difference in the quality of the diagnostic tests. | 18 months | |
Secondary | Is there a significant difference between the sensitivity and specificity of the 'rule of six' proposed in Mistry et al. 2016 and lumbar puncture with oligoclonal bands? | Comparison with past research | 18 months |
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