Information:
Error:
STATUS OF TREATMENT BLIND
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Was the treatment blind broken during the study?
Item
Was the treatment blind broken during the study?
boolean
C0749659 (UMLS CUI [1,1])
C2347038 (UMLS CUI [1,2])
C2347038 (UMLS CUI [1,2])
Date blind broken
Item
Date blind broken
datetime
C0011008 (UMLS CUI [1,1])
C2347038 (UMLS CUI [1,2])
C2347038 (UMLS CUI [1,2])
CL Item
Medical emergency requiring identification of investigation al product for further treatment (1)
C0013961 (UMLS CUI-1)
(Comment:en)
(Comment:en)
CL Item
Other, specify (2)
C1521902 (UMLS CUI-1)
(Comment:en)
(Comment:en)
PGx-PHARMACOGENETIC RESEARCH INSTRUCTIONS
Item
PGx-PHARMACOGENETIC RESEARCH INSTRUCTIONS
text
C0031325 (UMLS CUI [1,1])
C1442085 (UMLS CUI [1,2])
C1442085 (UMLS CUI [1,2])
CONSENT FOR PGx-PHARMACOGENETIC RESEARCH
Item
CONSENT FOR PGx-PHARMACOGENETIC RESEARCH
boolean
C0021430 (UMLS CUI [1,1])
C2347500 (UMLS CUI [1,2])
C2347500 (UMLS CUI [1,2])
If Yes, record the date informed consent obtained for PGx-Pharmacogenetic research
Item
If Yes, record the date informed consent obtained for PGx-Pharmacogenetic research
date
C2985782 (UMLS CUI [1])
CL Item
Subject declined (Subject declined)
CL Item
Subject not asked by Investigator (Subject not asked by Investigator)
CL Item
Other, specify (Other, specify)
BLOOD SAMPLE COLLECTION
Item
Has a blood sample been collected for PGx-pharmacogenetic research?
boolean
C0005834 (UMLS CUI [1])
If Yes, record the date sample taken
Item
If Yes, record the date sample taken
date
C0005834 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
WITHDRAWAL OF CONSENT
Item
Has subject withdrawn consent for PGx-Pharmacogenetic research?
boolean
C1707492 (UMLS CUI [1])
BLOOD SAMPLE DESTRUCTION
Item
BLOOD SAMPLE DESTRUCTION
boolean
C1948029 (UMLS CUI [1,1])
C0178913 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,2])
Item
If Yes: BLOOD SAMPLE DESTRUCTION
integer
C1948029 (UMLS CUI [1,1])
C0178913 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,2])
CL Item
Subject requested (1)
CL Item
Other, specify (2)
CONCOMITANT MEDICATIONS
Item
CONCOMITANT MEDICATIONS
text
C2347852 (UMLS CUI [1])
CL Item
Tablet (TAB)
C0039225 (UMLS CUI-1)
(Comment:en)
(Comment:en)
CL Item
Micro litre (MCL)
C1519795 (UMLS CUI-1)
(Comment:en)
(Comment:en)
CL Item
Millilitre (ML)
(Comment:en)
CL Item
Litre (L)
(Comment:en)
CL Item
Microgram (MCG)
(Comment:en)
CL Item
Milligram (MG)
(Comment:en)
CL Item
Gram (G)
(Comment:en)
CL Item
Optional therapeutic specific code (?)
(Comment:en)
CL Item
Optional therapeutic specific code (?)