ID

22328

Description

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 in/after Screening Period 1, Weeks 2, 1 Month +/- 3 Days, 2 Months, 4 Months, 6 Months +/- 1 week, 8 Months, 10 Months, 12 Months +/- 1 week and Follow Up. Sponsor: GSK Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT00265148?term=NCT00265148&rank=1

Lien

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

Mots-clés

  1. 30/05/2017 30/05/2017 -
  2. 30/05/2017 30/05/2017 -
Téléchargé le

30 mai 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Dosing and Compliance Effects of Rosiglitazone on Cerebral Glucose Utilization and Cognition in Subjects With Alzheimer's Disease NCT00265148

Dosing and Compliance Effects of Rosiglitazone on Cerebral Glucose Utilization and Cognition in Subjects With Alzheimer's Disease NCT00265148

Dosing Details
Description

Dosing Details

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C0178602
Date and time of dosing of Investigational product:
Description

Date and Time

Type de données

datetime

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0011008
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C0040223
Randomisation Number
Description

Randomisation Number

Type de données

float

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0237753
Investigational Product Compliance
Description

Investigational Product Compliance

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C1321605
Investigational Product (e.g Bottle 1)
Description

Investigational Product

Type de données

text

Alias
UMLS CUI [1]
C0304229
Start date
Description

Start date

Type de données

date

Unités de mesure
  • dd/mm/yy
Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0304229
dd/mm/yy
Stop Date
Description

Stop Date

Type de données

date

Unités de mesure
  • dd/mm/yy
Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C0304229
dd/mm/yy
IP Container No.
Description

IP Container No.

Type de données

float

Alias
UMLS CUI [1,1]
C0180098
UMLS CUI [1,2]
C0304229
Total number of Tablets Dispensed
Description

Total number of Tablets Dispensed

Type de données

float

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

Total number of Tablets Returned

Type de données

float

Alias
UMLS CUI [1,1]
C2699071
UMLS CUI [1,2]
C0039225
Has the subject missed investigational product for > 7 consecutive days?
Description

Discontinuation

Type de données

boolean

Alias
UMLS CUI [1,1]
C0457454
UMLS CUI [1,2]
C0304229

Similar models

Dosing and Compliance Effects of Rosiglitazone on Cerebral Glucose Utilization and Cognition in Subjects With Alzheimer's Disease NCT00265148

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Dosing Details
C0013227 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
Date and Time
Item
Date and time of dosing of Investigational product:
datetime
C0013227 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
Randomisation Number
Item
Randomisation Number
float
C0034656 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Item Group
Investigational Product Compliance
C0304229 (UMLS CUI-1)
C1321605 (UMLS CUI-2)
Investigational Product
Item
Investigational Product (e.g Bottle 1)
text
C0304229 (UMLS CUI [1])
Start date
Item
Start date
date
C0808070 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
IP Container No.
Item
IP Container No.
float
C0180098 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
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])
Discontinuation
Item
Has the subject missed investigational product for > 7 consecutive days?
boolean
C0457454 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])

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