Informatie:
Fout:
ID
30956
Beschrijving
Assessment of Patient Use of a New Device: RebiSmart; ODM derived from: https://clinicaltrials.gov/show/NCT01195870
Link
https://clinicaltrials.gov/show/NCT01195870
Trefwoorden
Versies (1)
- 07-07-18 07-07-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
7 juli 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Multiple Sclerosis NCT01195870
Eligibility Multiple Sclerosis NCT01195870
- StudyEvent: Eligibility
Similar models
Eligibility Multiple Sclerosis NCT01195870
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Multiple Sclerosis, Relapsing-Remitting
Item
have relapsing remitting multiple sclerosis
boolean
C0751967 (UMLS CUI [1])
Age
Item
between 18 to 65 years old inclusive
boolean
C0001779 (UMLS CUI [1])
Rebif prescribed | Therapeutic procedure Start Absent
Item
have been prescribed rebif for the first time but not yet started treatment
boolean
C0752980 (UMLS CUI [1,1])
C0278329 (UMLS CUI [1,2])
C0087111 (UMLS CUI [2,1])
C0439659 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
C0278329 (UMLS CUI [1,2])
C0087111 (UMLS CUI [2,1])
C0439659 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Other Coding
Item
rebismart as chosen device
boolean
C3846158 (UMLS CUI [1])
Review of Multiple Sclerosis Nurse
Item
be under review by ms nurse
boolean
C0699752 (UMLS CUI [1,1])
C0026769 (UMLS CUI [1,2])
C0028661 (UMLS CUI [1,3])
C0026769 (UMLS CUI [1,2])
C0028661 (UMLS CUI [1,3])
Informed Consent
Item
having given written informed consent to participate in the study
boolean
C0021430 (UMLS CUI [1])
Rebif Injection | Self Administration Absent
Item
injections of rebif given by someone other than the patient
boolean
C0752980 (UMLS CUI [1,1])
C1533685 (UMLS CUI [1,2])
C0036589 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C1533685 (UMLS CUI [1,2])
C0036589 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Other Coding | Visual Impairment | Physical impairment
Item
patients unable to use the rebismart device due to visual or physical impairment
boolean
C3846158 (UMLS CUI [1])
C3665347 (UMLS CUI [2])
C0231171 (UMLS CUI [3])
C3665347 (UMLS CUI [2])
C0231171 (UMLS CUI [3])
Informed Consent Unwilling
Item
patients unwilling to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,2])
Medical contraindication Rebif
Item
contra-indications to rebif as defined in the summary of product characteristics (spc).
boolean
C1301624 (UMLS CUI [1,1])
C0752980 (UMLS CUI [1,2])
C0752980 (UMLS CUI [1,2])
Hypersensitivity Antipyretics | Prophylactic treatment flu-like symptoms
Item
allergy to the antipyretic analgesics that will be advised as prophylaxis for flu-like symptoms
boolean
C0020517 (UMLS CUI [1,1])
C0003419 (UMLS CUI [1,2])
C0199176 (UMLS CUI [2,1])
C0392171 (UMLS CUI [2,2])
C0003419 (UMLS CUI [1,2])
C0199176 (UMLS CUI [2,1])
C0392171 (UMLS CUI [2,2])