ID

22765

Beschrijving

Study part: Run-In Screen Failure.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Trefwoorden

Versies (1)
  1. 11-06-17 11-06-17 -
Houder van rechten

GlaxoSmithKline

Geüploaded op

11 juni 2017

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY-NC 3.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

  • Nieuwste
  • Oudste
  • Populair
  • Nieuwste
    • Nieuwste
    • Oudste
    • Populair

Geen commentaren

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Run-In Screen Failure Mepolizumab HES NCT00086658

Engels

Run-In Screen Failure

1 Formulieren  
  1. StudyEvent: ODM
    1. Run-In Screen Failure
SCREEN FAILURE / RUN-IN FAILURE
Beschrijving

SCREEN FAILURE / RUN-IN FAILURE

Alias
UMLS CUI-1
C1710476
Subject Identifier
Beschrijving

Subject Identifier

Datatype

text

Alias
UMLS CUI [1]
C2348585
Was this subject a screen failure / run-in failure?
Beschrijving

Screen Failure

Datatype

boolean

Alias
UMLS CUI [1]
C1710476
If Yes, screen failure / run-in failure date
Beschrijving

date Screen Failure

Datatype

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C1710476
Primary reason Adverse event
Beschrijving

Record details on Non-Serious Adverse Events or Serious Adverse Event page(s) as appropriate.

Datatype

boolean

Alias
UMLS CUI [1,1]
C1549995
UMLS CUI [1,2]
C0877248
Primary reason Lost to follow-up
Beschrijving

primary reason Lost to follow-up

Datatype

boolean

Alias
UMLS CUI [1,1]
C1549995
UMLS CUI [1,2]
C1302313
Primary reason Protocol violation
Beschrijving

primary reason Protocol violation

Datatype

boolean

Alias
UMLS CUI [1,1]
C1549995
UMLS CUI [1,2]
C1709750
Primary reason Did not fulfil eligibility criteria
Beschrijving

primary reason eligibility criteria

Datatype

boolean

Alias
UMLS CUI [1,1]
C1549995
UMLS CUI [1,2]
C1516637
Other, specify
Beschrijving

Other

Datatype

text

Alias
UMLS CUI [1]
C0205394
Terug naar het begin van de pagina

Similar models

Run-In Screen Failure

1 Formulieren
  1. StudyEvent: ODM
    1. Run-In Screen Failure
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
SCREEN FAILURE / RUN-IN FAILURE
C1710476 (UMLS CUI-1)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Screen Failure
Item
Was this subject a screen failure / run-in failure?
boolean
C1710476 (UMLS CUI [1])
date Screen Failure
Item
If Yes, screen failure / run-in failure date
date
C0011008 (UMLS CUI [1,1])
C1710476 (UMLS CUI [1,2])
primary reason Adverse event
Item
Primary reason Adverse event
boolean
C1549995 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])
primary reason Lost to follow-up
Item
Primary reason Lost to follow-up
boolean
C1549995 (UMLS CUI [1,1])
C1302313 (UMLS CUI [1,2])
primary reason Protocol violation
Item
Primary reason Protocol violation
boolean
C1549995 (UMLS CUI [1,1])
C1709750 (UMLS CUI [1,2])
primary reason eligibility criteria
Item
Primary reason Did not fulfil eligibility criteria
boolean
C1549995 (UMLS CUI [1,1])
C1516637 (UMLS CUI [1,2])
Other
Item
Other, specify
text
C0205394 (UMLS CUI [1])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial