ID

23596

Description

Study part: Corticosteroid Medication Week 8. 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

  1. 09/07/2017 09/07/2017 -
Détendeur de droits

GlaxoSmithKline

Téléchargé le

9 juillet 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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Corticosteroid Medication Week 8 Mepolizumab HES NCT00086658

Corticosteroid Medication Week 8

CORTICOSTEROID MEDICATIONS
Description

CORTICOSTEROID MEDICATIONS

Alias
UMLS CUI-1
C0013227 (Pharmaceutical Preparations)
SNOMED
763158003
LOINC
LP100609-9
UMLS CUI-2
C0001617 (Adrenal Cortex Hormones)
SNOMED
21568003
LOINC
LP20687-7
Changes to the subject’s corticosteroid medications taken since the last visit in the Screening recorded in Corticosteroid Medication section?
Description

Corticosteroid Medication

Type de données

boolean

Alias
UMLS CUI [1,1]
C0013227 (Pharmaceutical Preparations)
SNOMED
763158003
LOINC
LP100609-9
UMLS CUI [1,2]
C0001617 (Adrenal Cortex Hormones)
SNOMED
21568003
LOINC
LP20687-7

Similar models

Corticosteroid Medication Week 8

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
CORTICOSTEROID MEDICATIONS
C0013227 (UMLS CUI-1)
C0001617 (UMLS CUI-2)
Corticosteroid Medication
Item
Changes to the subject’s corticosteroid medications taken since the last visit in the Screening recorded in Corticosteroid Medication section?
boolean
C0013227 (UMLS CUI [1,1])
C0001617 (UMLS CUI [1,2])

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