ID

22329

Beschrijving

A Double-blind, Randomized, Placebo-controlled, Parallel-group Study to Investigate the Effects of Rosiglitazone (Extended Release Tablets) on Cerebral Glucose Utilization and Cognition in Subjects With Mild to Moderate Alzheimer's Disease (AD) Medicine: rosiglitazone, Condition: Alzheimer's Disease, Phase: 2, Clinical Study ID: 49653/461, This form is to be performed after 2 weeks. Sponsor: GSK Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT00265148?term=NCT00265148&rank=1

Link

https://clinicaltrials.gov/ct2/show/NCT00265148?term=NCT00265148&rank=1

Trefwoorden

Versies (1)
  1. 30-05-17 30-05-17 -
Geüploaded op

30 mei 2017

DOI

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Licentie

Creative Commons BY-NC 3.0
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Baseline Signs and Symptoms Effects of Rosiglitazone on Cerebral Glucose Utilization and Cognition in Subjects With Alzheimer's Disease NCT00265148

Engels

Baseline Signs and Symptoms Effects of Rosiglitazone on Cerebral Glucose Utilization and Cognition in Subjects With Alzheimer's Disease NCT00265148

1 Formulieren  
Baseline Signs and Symptoms
Beschrijving

Baseline Signs and Symptoms

Alias
UMLS CUI-1
C0037088
If no baseline events experienced, please mark box and sign form below.
Beschrijving

baseline Event

Datatype

boolean

Alias
UMLS CUI [1]
C0037088
Baseline Signs and Symptoms
Beschrijving

Baseline Signs and Symptoms

Alias
UMLS CUI-1
C0877248
UMLS CUI-2
C0037088
Baseline Sign/Symptom GSK Use
Beschrijving

Diagnosis

Datatype

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0011900
Onset Date and Time
Beschrijving

Onset Date and Time

Datatype

datetime

Alias
UMLS CUI [1]
C2985916
Outcome *If subject died, please inform GSK within 24 hours and complete Form D
Beschrijving

Outcome

Datatype

integer

Alias
UMLS CUI [1]
C1705586
Event Course
Beschrijving

Course

Datatype

integer

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0750729
If intermittent, give No. of episodes
Beschrijving

Episode

Datatype

float

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C0332189
Intensity (maximum)
Beschrijving

Intensity

Datatype

integer

Alias
UMLS CUI [1,1]
C0522510
UMLS CUI [1,2]
C0877248
Relationship to study procedures performed prior to randomisation
Beschrijving

trial procedures

Datatype

integer

Alias
UMLS CUI [1,1]
C0008976
UMLS CUI [1,2]
C2700391
Corrective Therapy If ´Yes`, Please record on Prior Medication form.
Beschrijving

Corrective Therapy

Datatype

boolean

Alias
UMLS CUI [1]
C0087111
Was subject withdrawn due to this event?
Beschrijving

Withdrawal

Datatype

boolean

Alias
UMLS CUI [1]
C2349954
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Similar models

Baseline Signs and Symptoms Effects of Rosiglitazone on Cerebral Glucose Utilization and Cognition in Subjects With Alzheimer's Disease NCT00265148

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Baseline Signs and Symptoms
C0037088 (UMLS CUI-1)
baseline Event
Item
If no baseline events experienced, please mark box and sign form below.
boolean
C0037088 (UMLS CUI [1])
Item Group
Baseline Signs and Symptoms
C0877248 (UMLS CUI-1)
C0037088 (UMLS CUI-2)
Diagnosis
Item
Baseline Sign/Symptom GSK Use
text
C0877248 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
Onset Date and Time
Item
Onset Date and Time
datetime
C2985916 (UMLS CUI [1])
Item
Outcome *If subject died, please inform GSK within 24 hours and complete Form D
integer
C1705586 (UMLS CUI [1])
Outcome
Code List
Outcome *If subject died, please inform GSK within 24 hours and complete Form D
CL Item
Resolved (1)
CL Item
Ongoing (2)
CL Item
Died* (3)
Item
Event Course
integer
C0877248 (UMLS CUI [1,1])
C0750729 (UMLS CUI [1,2])
Course
Code List
Event Course
CL Item
Intermittent  (1)
CL Item
Constant (2)
Episode
Item
If intermittent, give No. of episodes
float
C0877248 (UMLS CUI [1,1])
C0332189 (UMLS CUI [1,2])
Item
Intensity (maximum)
integer
C0522510 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
Intensity
Code List
Intensity (maximum)
CL Item
Mild (1)
CL Item
Moderate (3)
CL Item
Severe (3)
Item
Relationship to study procedures performed prior to randomisation
integer
C0008976 (UMLS CUI [1,1])
C2700391 (UMLS CUI [1,2])
trial procedures
Code List
Relationship to study procedures performed prior to randomisation
CL Item
Not related (1)
CL Item
Unlikely (2)
CL Item
Suspected (reasonable possibility) (3)
CL Item
Probable (4)
Corrective Therapy
Item
Corrective Therapy If ´Yes`, Please record on Prior Medication form.
boolean
C0087111 (UMLS CUI [1])
Withdrawal
Item
Was subject withdrawn due to this event?
boolean
C2349954 (UMLS CUI [1])
Terug naar het begin van de pagina 

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