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Clinical Trials/EUCTR2006-001337-17-DE
EUCTR2006-001337-17-DE
Active, not recruiting
Not Applicable

Characterisation of multiple sclerosis pathology by ultra small particles of iron oxide (USPIO)” in comparison with conventional and advanced MRI imaging techniques[Charakterisierung der Multiple Sklerose Pathologie durch ultra small particles of iron oxide (USPIO)” im Vergleich zu konventionellen und fortgeschrittenen MRT Techniken] - MS_USPIO_MPIP

Max-Planck-Institute of Psychiatry0 sitesMarch 26, 2007

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Patients with Multiple Sclerosis (MS, N=90) and patients with a clinically isolated syndrome (ref. to as CIS in literature, i. e. not a clinically definite MS but a syndrome that may occur as first sign of MS early in the course, N=15) are planned to be investigated in the proposed clinical trial.
Sponsor
Max-Planck-Institute of Psychiatry
Status
Active, not recruiting
Last Updated
13 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 26, 2007
End Date
TBD
Last Updated
13 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Max-Planck-Institute of Psychiatry

Eligibility Criteria

Inclusion Criteria

  • a. clinically definite MS acc. to McDonald's criteria for the MS group (N\=90\)
  • b. clinically isolated syndrome compatible with MS, no definite diagnosis of MS (for CIS patients, N\=15\)
  • b. age over or equal 18 years
  • d. cognitive abilities to give informed consent
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range

Exclusion Criteria

  • a. Age below 18 years
  • b. Pregnancy
  • c. Withdrawal of consent
  • d. hypersensitivity to dextrane

Outcomes

Primary Outcomes

Not specified

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