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Laboratory Data Open-Label Extension Assessing Long-Term Safety Of Rosiglitazone In Subjects With Mild To Moderate Alzheimer's Disease NCT00381238

1 forms  
Investigational Product
Description

Investigational Product

Alias
UMLS CUI-1
C0304229
Has the subject missed investigational product for >7 days? (e.g Bottle 1)
Description

Investigational Product

Data type

boolean

Alias
UMLS CUI [1]
C0304229
Investigational Product (e.g Bottle A)
Description

Investigational Product

Data type

integer

Alias
UMLS CUI [1]
C0304229
Start Date (e.g. 05 Jun 02)
Description

Start Date

Data type

date

Measurement units
  • dd/MMM/yy
Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0808070
dd/MMM/yy
Stop Date (e.g. 10 Jun 02)
Description

Stop Date

Data type

date

Measurement units
  • dd/MMM/yy
Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0806020
dd/MMM/yy
Dose
Description

Dose

Data type

float

Measurement units
  • mg
Alias
UMLS CUI [1]
C3174092
mg
Compliance
Description

Compliance

Alias
UMLS CUI-1
C1321605
Total number of Tablets Dispensed
Description

Total number of Tablets Dispensed

Data type

float

Alias
UMLS CUI [1,1]
C0805077
UMLS CUI [1,2]
C0039225
Total number of Tablets Returned
Description

Total number of Tablets Returned

Data type

float

Alias
UMLS CUI [1,1]
C2699071
UMLS CUI [1,2]
C0039225
Treatment Confirmation
Description

Treatment Confirmation

Alias
UMLS CUI-1
C0750484
UMLS CUI-2
C0087111
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
Description

Therapeutic Procedures

Data type

boolean

Alias
UMLS CUI [1]
C0087111
If No, record reasons
Description

If No

Data type

text

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C2348235
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Similar models

Laboratory Data Open-Label Extension Assessing Long-Term Safety Of Rosiglitazone In Subjects With Mild To Moderate Alzheimer's Disease NCT00381238

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Investigational Product
C0304229 (UMLS CUI-1)
Investigational Product
Item
Has the subject missed investigational product for >7 days? (e.g Bottle 1)
boolean
C0304229 (UMLS CUI [1])
Item
Investigational Product (e.g Bottle A)
integer
C0304229 (UMLS CUI [1])
Investigational Product
Code List
Investigational Product (e.g Bottle A)
CL Item
Bottle A (1)
CL Item
Bottle B (2)
CL Item
Bottle C (3)
CL Item
Bottle D (4)
Start Date
Item
Start Date (e.g. 05 Jun 02)
date
C0304229 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Stop Date
Item
Stop Date (e.g. 10 Jun 02)
date
C0304229 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Dose
Item
Dose
float
C3174092 (UMLS CUI [1])
Item Group
Compliance
C1321605 (UMLS CUI-1)
Total number of Tablets Dispensed
Item
Total number of Tablets Dispensed
float
C0805077 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
Total number of Tablets Returned
Item
Total number of Tablets Returned
float
C2699071 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
Item Group
Treatment Confirmation
C0750484 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
Therapeutic Procedures
Item
Did the subject receive the correct treatment (e.g., treatment which the subject was assigned to) during this dosing interval?
boolean
C0087111 (UMLS CUI [1])
If No
Item
If No, record reasons
text
C0087111 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
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