ID

36510

Description

Baseline Cortical Haemodynamics in MS; ODM derived from: https://clinicaltrials.gov/show/NCT02481882

Link

https://clinicaltrials.gov/show/NCT02481882

Keywords

Versions (1)
  1. 5/18/19 5/18/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

May 18, 2019

DOI

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License

Creative Commons BY 4.0
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Eligibility Multiple Sclerosis NCT02481882

English

Eligibility Multiple Sclerosis NCT02481882

1 forms  
Criteria
Description

Criteria

male or female volunteers who are between the ages of 21 and 80.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
able to give voluntary written informed consent to participate in the study.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
able to understand the requirements of the study, including anonymous publication, and agree to co-operate with the study procedures.
Description

Comprehension Study Protocol | Protocol Compliance

Data type

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C2348563
UMLS CUI [2]
C0525058
inclusion criteria (patients):
Description

Inclusion criteria Patients

Data type

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0030705
diagnosed with multiple sclerosis.
Description

Multiple Sclerosis

Data type

boolean

Alias
UMLS CUI [1]
C0026769
male or female volunteers who are between the ages of 21 and 80.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
able to give voluntary written informed consent to participate in the study.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
able to understand the requirements of the study, including anonymous publication, and agree to co-operate with the study procedures.
Description

Comprehension Study Protocol | Protocol Compliance

Data type

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C2348563
UMLS CUI [2]
C0525058
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
any history of neurological illness other than ms.
Description

nervous system disorder | Exception Multiple Sclerosis

Data type

boolean

Alias
UMLS CUI [1]
C0027765
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0026769
known hypersensitivity to any mr or x-ray contrast agent.
Description

Contrast media allergy

Data type

boolean

Alias
UMLS CUI [1]
C0570562
any history of renal failure or disease.
Description

Kidney Failure | Kidney Disease

Data type

boolean

Alias
UMLS CUI [1]
C0035078
UMLS CUI [2]
C0022658
any history of allergies.
Description

Hypersensitivity

Data type

boolean

Alias
UMLS CUI [1]
C0020517
any history of circulation problems (vascular disease).
Description

Circulation problem | Vascular Disease

Data type

boolean

Alias
UMLS CUI [1]
C0848724
UMLS CUI [2]
C0042373
pregnancy or breastfeeding.
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
mri contraindications as screened on safety questionnaire (e.g. metal implants or pacemaker).
Description

Medical contraindication MRI | Metallic implant | Artificial cardiac pacemaker

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
UMLS CUI [2]
C3693688
UMLS CUI [3]
C0030163
have taken part in any other clinical study within the previous 3 months.#
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
any contraindications provided from mri, contrast agent and respiract safety forms.
Description

Medical contraindication MRI | Medical contraindication Contrast Media | Other Coding

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0009924
UMLS CUI [3]
C3846158
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Similar models

Eligibility Multiple Sclerosis NCT02481882

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Age
Item
male or female volunteers who are between the ages of 21 and 80.
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
able to give voluntary written informed consent to participate in the study.
boolean
C0021430 (UMLS CUI [1])
Comprehension Study Protocol | Protocol Compliance
Item
able to understand the requirements of the study, including anonymous publication, and agree to co-operate with the study procedures.
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2])
Inclusion criteria Patients
Item
inclusion criteria (patients):
boolean
C1512693 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
Multiple Sclerosis
Item
diagnosed with multiple sclerosis.
boolean
C0026769 (UMLS CUI [1])
Age
Item
male or female volunteers who are between the ages of 21 and 80.
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
able to give voluntary written informed consent to participate in the study.
boolean
C0021430 (UMLS CUI [1])
Comprehension Study Protocol | Protocol Compliance
Item
able to understand the requirements of the study, including anonymous publication, and agree to co-operate with the study procedures.
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
nervous system disorder | Exception Multiple Sclerosis
Item
any history of neurological illness other than ms.
boolean
C0027765 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C0026769 (UMLS CUI [2,2])
Contrast media allergy
Item
known hypersensitivity to any mr or x-ray contrast agent.
boolean
C0570562 (UMLS CUI [1])
Kidney Failure | Kidney Disease
Item
any history of renal failure or disease.
boolean
C0035078 (UMLS CUI [1])
C0022658 (UMLS CUI [2])
Hypersensitivity
Item
any history of allergies.
boolean
C0020517 (UMLS CUI [1])
Circulation problem | Vascular Disease
Item
any history of circulation problems (vascular disease).
boolean
C0848724 (UMLS CUI [1])
C0042373 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnancy or breastfeeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Medical contraindication MRI | Metallic implant | Artificial cardiac pacemaker
Item
mri contraindications as screened on safety questionnaire (e.g. metal implants or pacemaker).
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C3693688 (UMLS CUI [2])
C0030163 (UMLS CUI [3])
Study Subject Participation Status
Item
have taken part in any other clinical study within the previous 3 months.#
boolean
C2348568 (UMLS CUI [1])
Medical contraindication MRI | Medical contraindication Contrast Media | Other Coding
Item
any contraindications provided from mri, contrast agent and respiract safety forms.
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0009924 (UMLS CUI [2,2])
C3846158 (UMLS CUI [3])
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