ID

32557

Descripción

Study ID: 106837 Clinical Study ID: HZA106837 Study Title: A Long-Term, Randomized, Double-Blind, Parallel Group Study of Fluticasone Furoate/GW642444 Inhalation Powder Once-Daily and Fluticasone Furoate Inhalation Powder Once-Daily in Subjects with Asthma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01086384 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone furoate/vilanterol Trade Name: Relvar Study Indication: Asthma

Palabras clave

Versiones (2)
  1. 6/11/18 6/11/18 -
  2. 6/12/18 6/12/18 -
Titular de derechos de autor

GSK group of companies

Subido en

6 de noviembre de 2018

DOI

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Licencia

Creative Commons BY-NC 3.0
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A Parallel Group Study of Fluticasone Furoate/Vilanterol in Subjects with Asthma - 106837

Inglés

Study conclusion

1 formularios  
  1. StudyEvent: ODM
    1. Study conclusion
Study conclusion details
Descripción

Study conclusion details

Date of subject completion or withdrawal
Descripción

Date of subject completion or withdrawal

Tipo de datos

date

Was the subject withdrawn from the study?
Descripción

Was the subject withdrawn from the study?

Tipo de datos

boolean

If YES, complete primary reason for withdrawal
Descripción

If YES, complete primary reason for withdrawal

1. Adverse event
Descripción

record details on AE or SAE forms as appropriate)

Tipo de datos

boolean

2. Lack of efficacy
Descripción

Check all that apply. If none, select "No Subreasons"

Tipo de datos

text

3. Protocol Deviation
Descripción

Check all that apply. If none, select "No Subreasons"

Tipo de datos

text

4. Subject reached protocol defined stopping criteria
Descripción

4. Subject reached protocol defined stopping criteria

Tipo de datos

text

5. Study closed/terminated
Descripción

5. Study closed/terminated

Tipo de datos

boolean

6. Lost to Follow-Up
Descripción

6. Lost to Follow-Up

Tipo de datos

boolean

7. Investigator discretion, specify
Descripción

Select this reason if none of the other primary reasons are appropriate

Tipo de datos

text

8. Withdrew consent, specify
Descripción

Select this reason if none of the other primary reasons are appropriate

Tipo de datos

text

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Similar models

Study conclusion

1 formularios
  1. StudyEvent: ODM
    1. Study conclusion
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Study conclusion details
Date of subject completion or withdrawal
Item
Date of subject completion or withdrawal
date
Was the subject withdrawn from the study?
Item
Was the subject withdrawn from the study?
boolean
Item Group
If YES, complete primary reason for withdrawal
1. Adverse event
Item
1. Adverse event
boolean
Item
2. Lack of efficacy
text
2. Lack of efficacy
Code List
2. Lack of efficacy
CL Item
No subreasons (1)
CL Item
Exacerbation (2)
Item
3. Protocol Deviation
text
3. Protocol Deviation
Code List
3. Protocol Deviation
CL Item
No subreasons (1)
CL Item
Pregnancy (2)
CL Item
Lack of adherence (3)
CL Item
Prohibited medication use (4)
Item
4. Subject reached protocol defined stopping criteria
text
Subject reached protocol defined stopping criteria
Code List
4. Subject reached protocol defined stopping criteria
CL Item
Yes (1)
CL Item
No (2)
CL Item
Liver function test abnormality (3)
5. Study closed/terminated
Item
5. Study closed/terminated
boolean
6. Lost to Follow-Up
Item
6. Lost to Follow-Up
boolean
7. Investigator discretion, specify
Item
7. Investigator discretion, specify
text
8. Withdrew consent, specify
Item
8. Withdrew consent, specify
text
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