ID

22329

Beschreibung

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

Stichworte

Versionen (1)
  1. 30.05.17 30.05.17 -
Hochgeladen am

30. Mai 2017

DOI

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Lizenz

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

Englisch

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

1 Formulare  
Baseline Signs and Symptoms
Beschreibung

Baseline Signs and Symptoms

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

baseline Event

Datentyp

boolean

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

Baseline Signs and Symptoms

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

Diagnosis

Datentyp

text

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

Onset Date and Time

Datentyp

datetime

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

Outcome

Datentyp

integer

Alias
UMLS CUI [1]
C1705586
Event Course
Beschreibung

Course

Datentyp

integer

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

Episode

Datentyp

float

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

Intensity

Datentyp

integer

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

trial procedures

Datentyp

integer

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

Corrective Therapy

Datentyp

boolean

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Was subject withdrawn due to this event?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

Withdrawal

Datentyp

boolean

Alias
UMLS CUI [1]
C2349954
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Ähnliche Modelle

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

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])
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