ID

22764

Description

Study part: Corticosteroid Medication Screening to Randomization.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.

Mots-clés

Versions (1)
  1. 11.06.17 11.06.17 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

11. Juni 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0
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Corticosteroid Medication Screening to Randomization Mepolizumab HES NCT00086658

Anglais

Corticosteroid Medication Screening to Randomization

1 Formulaires  
SCREENING PERIOD CORTICOSTEROID MEDICATION
Description

SCREENING PERIOD CORTICOSTEROID MEDICATION

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C0001617
Subject ID
Description

Subject ID

Type de données

text

Alias
UMLS CUI [1]
C2348585
Was any Corticosteroid medication taken by the subject after the Screening Visit and prior to the first dose of study medication?
Description

Medication Corticosteroid

Type de données

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0001617
Drug Name
Description

Drug Name

Type de données

text

Alias
UMLS CUI [1]
C0013227
Total Daily Dose
Description

Total Daily Dose

Type de données

float

Alias
UMLS CUI [1]
C2348070
Units
Description

Unit Total Daily Dose

Type de données

text

Alias
UMLS CUI [1,1]
C0439148
UMLS CUI [1,2]
C2348070
Start Date
Description

Start Date

Type de données

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Description

Stop Date

Type de données

date

Alias
UMLS CUI [1]
C0806020
Ongoing Medication?
Description

Ongoing Medication

Type de données

boolean

Alias
UMLS CUI [1]
C2826666
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Similar models

Corticosteroid Medication Screening to Randomization

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
SCREENING PERIOD CORTICOSTEROID MEDICATION
C0013227 (UMLS CUI-1)
C0001617 (UMLS CUI-2)
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Medication Corticosteroid
Item
Was any Corticosteroid medication taken by the subject after the Screening Visit and prior to the first dose of study medication?
boolean
C0013227 (UMLS CUI [1,1])
C0001617 (UMLS CUI [1,2])
Drug Name
Item
Drug Name
text
C0013227 (UMLS CUI [1])
Total Daily Dose
Item
Total Daily Dose
float
C2348070 (UMLS CUI [1])
Unit Total Daily Dose
Item
Units
text
C0439148 (UMLS CUI [1,1])
C2348070 (UMLS CUI [1,2])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1])
Ongoing Medication
Item
Ongoing Medication?
boolean
C2826666 (UMLS CUI [1])
Retour au début de la page 

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