ID

36510

Description

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

Lien

https://clinicaltrials.gov/show/NCT02481882

Mots-clés

  1. 18/05/2019 18/05/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

18 mai 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Multiple Sclerosis NCT02481882

Eligibility Multiple Sclerosis NCT02481882

Criteria
Description

Criteria

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

Age

Type de données

boolean

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

Informed Consent

Type de données

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

Type de données

boolean

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

Inclusion criteria Patients

Type de données

boolean

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

Multiple Sclerosis

Type de données

boolean

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

Age

Type de données

boolean

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

Informed Consent

Type de données

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

Type de données

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

Type de données

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

Type de données

boolean

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

Kidney Failure | Kidney Disease

Type de données

boolean

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

Hypersensitivity

Type de données

boolean

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

Circulation problem | Vascular Disease

Type de données

boolean

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

Pregnancy | Breast Feeding

Type de données

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

Type de données

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

Type de données

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

Type de données

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

Similar models

Eligibility Multiple Sclerosis NCT02481882

Name
Type
Description | Question | Decode (Coded Value)
Type de données
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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