Informationen:
Fehler:
ID
15640
Beschreibung
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 Part: Baseline 1st cycle Trial Medication
Link
https://clinicaltrials.gov/ct2/show/NCT02419378
Stichworte
Versionen (5)
- 13.08.15 13.08.15 - Martin Dugas
- 23.05.16 23.05.16 -
- 28.05.16 28.05.16 -
- 28.05.16 28.05.16 -
- 06.06.16 06.06.16 -
Hochgeladen am
6. Juni 2016
DOI
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Lizenz
Creative Commons BY 4.0
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Baseline 1st cycle Trial Medication Multiple Sclerosis ALAIN01 NCT02419378
Baseline 1st cycle Trial Medication Multiple Sclerosis ALAIN01 NCT02419378
Ähnliche Modelle
Baseline 1st cycle Trial Medication Multiple Sclerosis ALAIN01 NCT02419378
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Patient ID (derived)
Item
Patient ID (derived)
text
C2348585 (UMLS CUI [1])
Trial Medication: Deferral Comment
Item
Trial Medication: Deferral Comment
text
C0205421 (UMLS CUI [1,1])
C0947611 (UMLS CUI [1,2])
C0947611 (UMLS CUI [1,2])
CL Item
Test not done (0)
CL Item
Test done (1)
Item
Trial Medication: Pregnancy Test, Kind of test
text
C0032976 (UMLS CUI [1,1])
C1550373 (UMLS CUI [1,2])
C1550373 (UMLS CUI [1,2])
Code List
Trial Medication: Pregnancy Test, Kind of test
CL Item
blood (1)
CL Item
urine (2)
Trial Medication Pregnancy Test: Date
Item
Trial Medication Pregnancy Test: Date
date
C0032976 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
Item
Trial MedicationI Pregnancy Test: Result
text
C0032976 (UMLS CUI [1,1])
C0243095 (UMLS CUI [1,2])
C0243095 (UMLS CUI [1,2])
CL Item
negative (0)
CL Item
positive (1)
Item
Trial Medication Pregnancy Test: Reason
text
C0032976 (UMLS CUI [1,1])
C0032976 (UMLS CUI [1,2])
C0032976 (UMLS CUI [1,2])
CL Item
no childbearing potential (0)
CL Item
other (9)
Pregnancy Test: Reason, Text
Item
Trial Medication Pregnancy Test: Reason, Text
text
C0032976 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,2])
Date of Signature
Item
Trial Medication: Date of Signature
date
C1519316 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
Item
Trial Medication: Signature yes/no
text
C1519316 (UMLS CUI [1,1])
C1705848 (UMLS CUI [1,2])
C1705848 (UMLS CUI [1,2])
CL Item
yes (1)
CL Item
no (0)
Comment
Item
Comment Trial Medication
text
C0947611 (UMLS CUI [1])
Date of Administration
Item
Trial Medication: Date of Administration
date
C1533734 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
Medication dose
Item
Trial Medication: Dose administered
float
C3174092 (UMLS CUI [1])
Batch Number
Item
Trial Medication: Batch No
text
C3641829 (UMLS CUI [1])
Expiration
Item
Trial Medication: Expiry Date
date
C3669020 (UMLS CUI [1])
Trial Medication: Reason if less than 12 mg
Item
Trial Medication: Reason if less than 12 mg
text
C3174092 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])