Informações:
Falhas:
ID
23003
Descrição
Study ID: 100527 Clinical Study ID: B2E100527 Study Title: A randomised, double blind, placebo controlled, parellel group study to examine the efficacy, safety, tolerability and systemic pharmacokinetic profile of repeated inhaled doses of GSK159797 Sponsor: GlaxoSmithKline Phase: phase 2 Study Recruitment Status: Completed Generic Name: milveterol Trade Name: Milveterol Study Indication: Pulmonary Disease, Chronic Obstructive
Palavras-chave
Versões (1)
- 19/06/2017 19/06/2017 -
Transferido a
19 de junho de 2017
DOI
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Licença
Creative Commons BY-NC 3.0
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Pharmacogenetic Research - GSK Milveterol COPD 100527
Pharmacogenetic Research - GSK Milveterol COPD 100527
- StudyEvent: ODM
Similar models
Pharmacogenetic Research - GSK Milveterol COPD 100527
- StudyEvent: ODM
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Consent for Pharmacogenetic Research
C0031325 (UMLS CUI-1)
C0021430 (UMLS CUI-2)
C0021430 (UMLS CUI-2)
Informed consent Pharmacogenetic Research
Item
Has informed consent been obtained for Pharmacogenetic Research?
boolean
C0031325 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
Date of consent
Item
lf 'Yes', date informed consent obtained for Pharmacogenetic Research:
date
C2985782 (UMLS CUI [1])
Item
If 'No', specify reason below:
text
C0566251 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C1705492 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C1705492 (UMLS CUI [1,3])
CL Item
Subject declined (Subject declined)
CL Item
Subject not asked by investigator (Subject not asked by investigator)
CL Item
Other (Other)
blood sample collected for Pharmacogenetic Research
Item
Has a blood sample been collected for Pharmacogenetic Research?
boolean
C0005834 (UMLS CUI [1,1])
C0031325 (UMLS CUI [1,2])
C0031325 (UMLS CUI [1,2])
Date of blood collection
Item
If 'Yes', date sample taken:
date
C1302413 (UMLS CUI [1])
withdraw consent
Item
Has this subject withdrawn consent for Pharmacogenetic Research?
boolean
C2349954 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])
Item Group
Blood Sample Destruction
C1948029 (UMLS CUI-1)
C0178913 (UMLS CUI-2)
C0178913 (UMLS CUI-2)
request sample destruction
Item
Has a request been made for sample destruction?
boolean
C1272683 (UMLS CUI [1,1])
C1948029 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,3])
C1948029 (UMLS CUI [1,2])
C0178913 (UMLS CUI [1,3])
Item
If 'Yes', one reason:
integer
C0566251 (UMLS CUI [1,1])
C1272683 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,4])
C1272683 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C0178913 (UMLS CUI [1,4])
CL Item
Subject's request (1)
CL Item
Screen failure (2)
CL Item
Other (3)