Inglés

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

1 formularios  
Investigational Product
Descripción

Investigational Product

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

Investigational Product

Tipo de datos

boolean

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

Investigational Product

Tipo de datos

integer

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

Start Date

Tipo de datos

date

Unidades de medida
  • dd/MMM/yy
Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0808070
dd/MMM/yy
Stop Date (e.g. 10 Jun 02)
Descripción

Stop Date

Tipo de datos

date

Unidades de medida
  • dd/MMM/yy
Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0806020
dd/MMM/yy
Dose
Descripción

Dose

Tipo de datos

float

Unidades de medida
  • mg
Alias
UMLS CUI [1]
C3174092
mg
Compliance
Descripción

Compliance

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

Total number of Tablets Dispensed

Tipo de datos

float

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

Total number of Tablets Returned

Tipo de datos

float

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

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?
Descripción

Therapeutic Procedures

Tipo de datos

boolean

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

If No

Tipo de datos

text

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C2348235
Volver a la parte superior de la página

Similar models

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

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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])
Volver a la parte superior de la página