ID

36495

Beschreibung

Rotating Frame Relaxation Imaging in Patients With Multiple Sclerosis; ODM derived from: https://clinicaltrials.gov/show/NCT02403570

Link

https://clinicaltrials.gov/show/NCT02403570

Stichworte

  1. 17.05.19 17.05.19 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

17. Mai 2019

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Multiple Sclerosis NCT02403570

Eligibility Multiple Sclerosis NCT02403570

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
the diagnosis of relapsing remitting ms made according to the poser, mcdonald's or revised mcdonald's criteria (group i) before participating in the study
Beschreibung

Multiple Sclerosis, Relapsing-Remitting

Datentyp

boolean

Alias
UMLS CUI [1]
C0751967
initial ms diagnosis of relapsing remitting form of the disease according to the criteria as mentioned above, and conversion into the secondary progressive phase of the disease as evaluated by the referring neurologist according to the clinical evaluation and confirmed by the study physician (group ii).
Beschreibung

Relapsing-Remitting Multiple Sclerosis Initial | Conversion | Multiple Sclerosis, Secondary Progressive

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0751967
UMLS CUI [1,2]
C0205265
UMLS CUI [2]
C0439836
UMLS CUI [3]
C0751965
mental status: patients must be able to understand the meaning of the study
Beschreibung

Mental state | Comprehension Study Protocol

Datentyp

boolean

Alias
UMLS CUI [1]
C0278060
UMLS CUI [2,1]
C0162340
UMLS CUI [2,2]
C2348563
informed consent: the patient must sign the appropriate ethical committee (ec) approved informed consent documents in the presence of the designated staff
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
any other autoimmune disease than ms requiring immunomodulatory or immunosuppressive medication
Beschreibung

Autoimmune Disease Requirement Biological Response Modifiers | Autoimmune Disease Requirement Immunosuppressive Agents | Exception Multiple Sclerosis

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0004364
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0005525
UMLS CUI [2,1]
C0004364
UMLS CUI [2,2]
C1514873
UMLS CUI [2,3]
C0021081
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C0026769
high-dose corticosteroid treatment within 30 days before participating in the study
Beschreibung

Steroid therapy High dose

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0149783
UMLS CUI [1,2]
C0444956
prior medical history: patient must have no history of serious cardiovascular, liver or kidney disease
Beschreibung

Cardiovascular Disease Serious | Liver disease Serious | Kidney Disease Serious

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0007222
UMLS CUI [1,2]
C0205404
UMLS CUI [2,1]
C0023895
UMLS CUI [2,2]
C0205404
UMLS CUI [3,1]
C0022658
UMLS CUI [3,2]
C0205404
any psychiatric condition that compromises the subject's ability to participate in the study
Beschreibung

Mental condition compromises Study Subject Participation Status

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3840291
UMLS CUI [1,2]
C2945640
UMLS CUI [1,3]
C2348568
infections: patient must not have an uncontrolled serious infection
Beschreibung

Communicable Disease Serious Uncontrolled

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0009450
UMLS CUI [1,2]
C0205404
UMLS CUI [1,3]
C0205318
no contraindications for mri (cardiac pacemaker, intracranial clips etc)
Beschreibung

Medical contraindication MRI | Artificial cardiac pacemaker | Clips Intracranial

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
UMLS CUI [2]
C0030163
UMLS CUI [3,1]
C0175722
UMLS CUI [3,2]
C0524466

Ähnliche Modelle

Eligibility Multiple Sclerosis NCT02403570

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Multiple Sclerosis, Relapsing-Remitting
Item
the diagnosis of relapsing remitting ms made according to the poser, mcdonald's or revised mcdonald's criteria (group i) before participating in the study
boolean
C0751967 (UMLS CUI [1])
Relapsing-Remitting Multiple Sclerosis Initial | Conversion | Multiple Sclerosis, Secondary Progressive
Item
initial ms diagnosis of relapsing remitting form of the disease according to the criteria as mentioned above, and conversion into the secondary progressive phase of the disease as evaluated by the referring neurologist according to the clinical evaluation and confirmed by the study physician (group ii).
boolean
C0751967 (UMLS CUI [1,1])
C0205265 (UMLS CUI [1,2])
C0439836 (UMLS CUI [2])
C0751965 (UMLS CUI [3])
Mental state | Comprehension Study Protocol
Item
mental status: patients must be able to understand the meaning of the study
boolean
C0278060 (UMLS CUI [1])
C0162340 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
Informed Consent
Item
informed consent: the patient must sign the appropriate ethical committee (ec) approved informed consent documents in the presence of the designated staff
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Autoimmune Disease Requirement Biological Response Modifiers | Autoimmune Disease Requirement Immunosuppressive Agents | Exception Multiple Sclerosis
Item
any other autoimmune disease than ms requiring immunomodulatory or immunosuppressive medication
boolean
C0004364 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0005525 (UMLS CUI [1,3])
C0004364 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0021081 (UMLS CUI [2,3])
C1705847 (UMLS CUI [3,1])
C0026769 (UMLS CUI [3,2])
Steroid therapy High dose
Item
high-dose corticosteroid treatment within 30 days before participating in the study
boolean
C0149783 (UMLS CUI [1,1])
C0444956 (UMLS CUI [1,2])
Cardiovascular Disease Serious | Liver disease Serious | Kidney Disease Serious
Item
prior medical history: patient must have no history of serious cardiovascular, liver or kidney disease
boolean
C0007222 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0023895 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C0022658 (UMLS CUI [3,1])
C0205404 (UMLS CUI [3,2])
Mental condition compromises Study Subject Participation Status
Item
any psychiatric condition that compromises the subject's ability to participate in the study
boolean
C3840291 (UMLS CUI [1,1])
C2945640 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
Communicable Disease Serious Uncontrolled
Item
infections: patient must not have an uncontrolled serious infection
boolean
C0009450 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0205318 (UMLS CUI [1,3])
Medical contraindication MRI | Artificial cardiac pacemaker | Clips Intracranial
Item
no contraindications for mri (cardiac pacemaker, intracranial clips etc)
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C0030163 (UMLS CUI [2])
C0175722 (UMLS CUI [3,1])
C0524466 (UMLS CUI [3,2])

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