Informatie:
Fout:
ID
36510
Beschrijving
Baseline Cortical Haemodynamics in MS; ODM derived from: https://clinicaltrials.gov/show/NCT02481882
Link
https://clinicaltrials.gov/show/NCT02481882
Trefwoorden
Versies (1)
- 18-05-19 18-05-19 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
18 mei 2019
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility Multiple Sclerosis NCT02481882
Eligibility Multiple Sclerosis NCT02481882
- StudyEvent: Eligibility
Similar models
Eligibility Multiple Sclerosis NCT02481882
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
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])
C2348563 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2])
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])
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])
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])
C0042373 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnancy or breastfeeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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])
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])
C0024485 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0009924 (UMLS CUI [2,2])
C3846158 (UMLS CUI [3])