ID

15354

Description

Alemtuzumab in Autoimmune Inflammatory Neurodegeneration: Mechanisms of Action and Neuroprotective Potential (ALAIN01) https://clinicaltrials.gov/ct2/show/NCT02419378 Principal Investigator Prof. Dr. Dr. Sven Meuth, University Hospital Muenster, Germany

Link

https://clinicaltrials.gov/ct2/show/NCT02419378

Keywords

  1. 8/13/15 8/13/15 - Martin Dugas
  2. 5/23/16 5/23/16 -
  3. 5/28/16 5/28/16 -
Uploaded on

May 28, 2016

DOI

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License

Creative Commons BY 4.0

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Discontinue Trial Medication Multiple Sclerosis ALAIN01 NCT02419378

Discontinue Trial Medication Multiple Sclerosis ALAIN01 NCT02419378

Discontinue Trial Medication
Description

Discontinue Trial Medication

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C0457454
Patient ID (derived)
Description

Patient ID (derived)

Data type

text

Alias
UMLS CUI [1]
C2348585
Discont. of Trial Medication: Date
Description

Discont. of Trial Medication: Date

Data type

date

Alias
UMLS CUI [1,1]
C1521826
UMLS CUI [1,2]
C0806020
If other reason was selected, please specify
Description

Other reason

Data type

text

Alias
UMLS CUI [1]
C3840932
Reason for discontinuation
Description

Reason for discontinuation

Data type

integer

Alias
UMLS CUI [1,1]
C0566251
UMLS CUI [1,2]
C0457454
Discont. of Trial Medication: Reason Text
Description

Discont. of Trial Medication: Reason Text

Data type

text

Alias
UMLS CUI [1,1]
C0457454
UMLS CUI [1,2]
C0566251
Discont. of Trial Medication: Date of Signature
Description

Date of Signature

Data type

date

Alias
UMLS CUI [1,1]
C1519316
UMLS CUI [1,2]
C0011008

Similar models

Discontinue Trial Medication Multiple Sclerosis ALAIN01 NCT02419378

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Discontinue Trial Medication
C0013227 (UMLS CUI-1)
C0457454 (UMLS CUI-2)
Patient ID (derived)
Item
Patient ID (derived)
text
C2348585 (UMLS CUI [1])
Trial medication end date
Item
Discont. of Trial Medication: Date
date
C1521826 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Other reason
Item
If other reason was selected, please specify
text
C3840932 (UMLS CUI [1])
Item
Reason for discontinuation
integer
C0566251 (UMLS CUI [1,1])
C0457454 (UMLS CUI [1,2])
Code List
Reason for discontinuation
CL Item
Investigator considers it would be in the best interests of the patient (1)
CL Item
Unacceptable toxicity of the study drug (2)
CL Item
HIV infection (3)
CL Item
Patient requests discontinuation (4)
CL Item
Patient is unable or unwilling to comply with planned study safety monitoring (5)
CL Item
Other reason: ____________ (6)
Discontinuation reason
Item
Discont. of Trial Medication: Reason Text
text
C0457454 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
Date of Signature
Item
Discont. of Trial Medication: Date of Signature
date
C1519316 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])

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