Centralized Reading Assessment of Chronic CerebroSpinal Venous Insufficiency (CCSVI) in Patients With Multiple Sclerosis and Other Neurological Diseases

University at Buffalo

Status: Completed

Conditions: Other Neurological Disorders (OND); Healthy (HC); Multiple Sclerosis (MS); Clinically Isolated Syndrome (CIS)

Study type: Observational

Funder types: Other

Identifiers

NCT02308579

CDUS1

Details and patient eligibility

About

This a retrospective, blinded trial in which collaborators in Italy will review the doppler findings from the Combined Transcranial and Extracranial Venous Doppler (CTEVD) trial in an attempt to measure reproducibility.

Full description

This study will retrospectively investigate doppler images from the second phase of the CTEVD trial.

1. To determine the prevalence of CCSVI in patients with MS, compared with the prevalence observed in a control population consisting of Other Neurological Diseases (OND) patients and Healthy Controls (HC) by using blinded, controlled centralized ultrasound reading assessment of 5 Venous Haemodynamic (VH) CCSVI CCSVI Doppler UltraSound (CDUS) criteria.
2. To investigate whether prevalence of CCSVI is different between centralized and local CDUS reading of 5 VH CCSVI CDUS criteria.
3. To investigate the prevalence of CCSVI in patients with MS, compared with the prevalence observed in a control population consisting of OND patients and HC, when bidirectional flow in the intracranial veins and sinuses CDUS criterion is not considered as part of VH CCSVI CDUS criteria.
4. To determine whether prevalence of CCSVI in patients with MS, compared with the prevalence observed in a control population consisting of OND patients and HC differs when using CDUS velocity and flow parameters in the Internal Jugular Veins (IJVs) and Vertebral Veins (VVs).
5. To determine the reproducibility of VH criteria by using of centralized and local blinded, controlled CDUS reading assessment.

Enrollment: 499 patients

Sex: All

Ages: 5 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Participation in the CTEVD Phase 2 study
• Available CDUS exam
• Diagnosed with CIS, MS, OND, or being a HC
• Fulfilling inclusion criteria from the CTEVD study

Exclusion criteria

• Not having an available CDUS exam
• Diagnosed with Radiologically Isolated Syndrome (RIS) or Neuromyelitis Optic (NMO)
• Fulfilling exclusion criteria from the CTEVD study

Trial design

499 participants in 4 patient groups

Multiple Sclerosis

Description:

Patients diagnosed with Multiple Sclerosis (MS), identified in the CTEVD trial

Clinically Isolated Syndrome

Description:

Patients diagnosed with Clinically Isolated Syndrome (CIS), identified in the CTEVD trial.

Other Neurological Disorders

Description:

Patients diagnosed with Other Neurological Disorders (OND), identified in the CTEVD trial. ONDs fall into one of four categories: Neurodegenerative, Vascular, Autoimmune, and Neuromuscular; and the following disorders: Acute Disseminated Encephalomyelitis (ADEM); Antiphospholipid Antibody (syndrome; APLA); Atypical, short-lasting neurodegenerative disease; Autoimmune disease not otherwise specified (NOS); Cerebellum Syndrome; Charcot-Marie Tooth Disease; Chiari Malformation; Chronic Fatigue Syndrome; Central Nervous System Vasculitis; Demyelinating Disease; Epilepsy; Headaches; Idiopathic Chronic Neuropathy; Migraines; Mitochondrial Disease; Myelopathy; Neurofibromatosis; Neuropathy; Optic Neuritis; Parasthesia related to Transient Ischemic Attacks (TIA); Parkinson's Disease; Restless legs syndrome; Seizures; Spinal Cerebellum Disease; Spinal Disc Degeneration; Syringomyelia; and Vertigo

Healthy Controls

Description:

Individuals who are healthy (i.e., free from neurological conditions; HC) , identified in the CTEVD trial.