ID

32494

Descrizione

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

Keywords

versioni (2)
  1. 05/11/18 05/11/18 -
  2. 30/11/18 30/11/18 -
Titolare del copyright

GSK group of companies

Caricato su

5 novembre 2018

DOI

Per favore, per richiedere un accesso.

Licenza

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

Inglese

Non-Serious Adverse Event Form

1 moduli  
Non-Serious Adverse Event (AE)
Descrizione

Non-Serious Adverse Event (AE)

Sequence Number
Descrizione

Sequence Number

Tipo di dati

integer

Event
Descrizione

Diagnosis Only (if known) Otherwise Sign/Symptom

Tipo di dati

text

Modified Term
Descrizione

Modified Term

Tipo di dati

text

Start Date
Descrizione

Start Date

Tipo di dati

date

End Date
Descrizione

End Date

Tipo di dati

date

Outcome
Descrizione

Outcome

Tipo di dati

text

Frequency
Descrizione

Frequency

Tipo di dati

text

Maximum Intensity
Descrizione

Record maximum intensity throughout duration of event

Tipo di dati

text

Intensity at onset of event
Descrizione

Intensity at onset of event

Tipo di dati

text

Maximum Grade
Descrizione

Maximum Grade

Tipo di dati

text

Grade at onset of event
Descrizione

Grade at onset of event

Tipo di dati

text

Maximum Grade or Intensity
Descrizione

Maximum Grade or Intensity

Tipo di dati

text

Grade or Intensity at onset of event
Descrizione

Grade or Intensity at onset of event

Tipo di dati

text

Action Taken with Investigational Product(s) as a result of the AE
Descrizione

Action Taken with Investigational Product(s) as a result of the AE

Tipo di dati

text

Did the subject withdraw from study as a result of this AE?
Descrizione

Did the subject withdraw from study as a result of this AE?

Tipo di dati

boolean

Is there a reasonable possibility that the AE may have been caused by the investigational product?
Descrizione

Ue best judgement at initial entry. May be amended when additional information becomes available.

Tipo di dati

boolean

Duration of AE if < 24 hours
Descrizione

HH:MM

Tipo di dati

integer

Time to Onset Since Last Dose
Descrizione

Time to Onset Since Last Dose

Tipo di dati

time

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Similar models

Non-Serious Adverse Event Form

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Non-Serious Adverse Event (AE)
Sequence Number
Item
Sequence Number
integer
Event
Item
Event
text
Modified Term
Item
Modified Term
text
Start Date
Item
Start Date
date
End Date
Item
End Date
date
Item
Outcome
text
Outcome
Code List
Outcome
CL Item
Recovered/Resolved (1)
CL Item
Recovering/Resolving (2)
CL Item
Not recovered/Not resolved (3)
CL Item
Recovered/Resolved with sequelae (4)
Item
Frequency
text
Frequency
Code List
Frequency
CL Item
Single Episode (1)
CL Item
Intermittent (2)
Item
Maximum Intensity
text
Maximum Intensity
Code List
Maximum Intensity
CL Item
[1] Mild (1)
CL Item
[2] Moderate (2)
CL Item
[3] Severe (3)
CL Item
[X] Not applicable (4)
Item
Intensity at onset of event
text
Intensity at onset of event
Code List
Intensity at onset of event
CL Item
[1] Mild (1)
CL Item
[2] Moderate (2)
CL Item
[3] Severe (3)
CL Item
[X] Not applicable (4)
Item
Maximum Grade
text
Maximum Grade
Code List
Maximum Grade
CL Item
Grade 1 (1)
CL Item
Grade 2 (2)
CL Item
Grade 3 (3)
CL Item
Grade 4 (4)
Item
Grade at onset of event
text
Grade at onset of event
Code List
Grade at onset of event
CL Item
Grade 1 (1)
CL Item
Grade 2 (2)
CL Item
Grade 3 (3)
CL Item
Grade 4 (4)
CL Item
Grade 5 (5)
Item
Maximum Grade or Intensity
text
Maximum Grade or Intensity
Code List
Maximum Grade or Intensity
CL Item
[1] Mild or Grade 1 (1)
CL Item
[2] Moderate or Grade 2 (2)
CL Item
[3] Severe or Grade 3 (3)
CL Item
[4] Grade 4 (4)
CL Item
[5] Grade 5 (5)
CL Item
[X] Not applicable (6)
Item
Grade or Intensity at onset of event
text
Grade or Intensity at onset of event
Code List
Grade or Intensity at onset of event
CL Item
[1] Mild or Grade 1 (1)
CL Item
[2] Moderate or Grade 2 (2)
CL Item
[3] Severe or Grade 3 (3)
CL Item
[4] Grade 4 (4)
CL Item
[5] Grade 5 (5)
CL Item
[X] Not applicable (6)
Item
Action Taken with Investigational Product(s) as a result of the AE
text
Action Taken with Investigational Product(s) as a result of the AE
Code List
Action Taken with Investigational Product(s) as a result of the AE
CL Item
[1] Investigational product(s) withdrawn (1)
CL Item
[2] Dose reduced (2)
CL Item
[3] Dose increased (3)
CL Item
[4] Dose not changed (4)
CL Item
[5] Dose interrupted (5)
CL Item
[X] Not applicable (6)
Did the subject withdraw from study as a result of this AE?
Item
Did the subject withdraw from study as a result of this AE?
boolean
Is there a reasonable possibility that the AE may have been caused by the investigational product?
Item
Is there a reasonable possibility that the AE may have been caused by the investigational product?
boolean
Duration of AE if < 24 hours
Item
Duration of AE if < 24 hours
integer
Time to Onset Since Last Dose
Item
Time to Onset Since Last Dose
time
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