ID

22171

Descrição

This is an open-label extension to study 49653/461, to assess the long-term safety of rosiglitazone (extended release tablets) in subjects with mild to moderate Alzheimer's Disease. GSK Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT00381238?term=NCT00381238&rank=1

Link

https://clinicaltrials.gov/ct2/show/NCT00381238?term=NCT00381238&rank=1

Palavras-chave

  1. 09/05/2017 09/05/2017 -
  2. 22/05/2017 22/05/2017 -
Transferido a

22 de maio de 2017

DOI

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Licença

Creative Commons BY-NC 3.0

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

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

Investigational Product Discontinuation - Rosiglitazone
Descrição

Investigational Product Discontinuation - Rosiglitazone

Alias
UMLS CUI-1
C0013230
UMLS CUI-2
C0457454
Was the investigational product stopped permanently before the end of the scheduled treatment period?
Descrição

Investigational Product

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0304229
If Yes, check the primary reason the investigational product was stopped:
Descrição

Discontinuation

Tipo de dados

integer

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0457454
Specify other:
Descrição

Specification other

Tipo de dados

text

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C2348235

Similar models

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

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Investigational Product Discontinuation - Rosiglitazone
C0013230 (UMLS CUI-1)
C0457454 (UMLS CUI-2)
Investigational Product
Item
Was the investigational product stopped permanently before the end of the scheduled treatment period?
boolean
C0304229 (UMLS CUI [1])
Item
If Yes, check the primary reason the investigational product was stopped:
integer
C0304229 (UMLS CUI [1,1])
C0457454 (UMLS CUI [1,2])
Code List
If Yes, check the primary reason the investigational product was stopped:
CL Item
Adverse Event (1)
CL Item
Lost to follow-up (2)
CL Item
Protocol violation (3)
CL Item
Subject decided to withdraw from the study (4)
CL Item
Lack of efficacy (5)
CL Item
Sponsor terminated study (6)
CL Item
Disease progression (7)
CL Item
Other, specify (8)
Specification other
Item
Specify other:
text
C0304229 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])

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