ID

22753

Description

Study part: CT Scans Day 1 Pre-Infusion.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.

Keywords

  1. 6/11/17 6/11/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

June 11, 2017

DOI

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License

Creative Commons BY-NC 3.0

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CT Scans Day 1 Pre-Infusion Mepolizumab HES NCT00086658

CT Scans Day 1 Pre-Infusion

CT SCANS
Description

CT SCANS

Alias
UMLS CUI-1
C0040405
Subject Identifier
Description

Subject Identifier

Data type

text

Alias
UMLS CUI [1]
C2348585
Date of assessment
Description

Date of assessment

Data type

date

Alias
UMLS CUI [1]
C2985720
Was the CT scan of the abdomen complete?
Description

CT abdomen

Data type

boolean

Alias
UMLS CUI [1]
C0412620
Was the CT scan of the chest complete?
Description

CT chest

Data type

boolean

Alias
UMLS CUI [1]
C0202823
Was the CT scan of the sinus complete?
Description

CT sinus

Data type

boolean

Alias
UMLS CUI [1]
C1660790

Similar models

CT Scans Day 1 Pre-Infusion

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
CT SCANS
C0040405 (UMLS CUI-1)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Date of assessment
Item
Date of assessment
date
C2985720 (UMLS CUI [1])
CT abdomen
Item
Was the CT scan of the abdomen complete?
boolean
C0412620 (UMLS CUI [1])
CT chest
Item
Was the CT scan of the chest complete?
boolean
C0202823 (UMLS CUI [1])
CT sinus
Item
Was the CT scan of the sinus complete?
boolean
C1660790 (UMLS CUI [1])

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