ID

23833

Description

Study part: 12-Lead ECG Week 38/ Early Withdrawal visit. 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. 7/15/17 7/15/17 -
Copyright Holder

GlaxoSmithKline

Uploaded on

July 15, 2017

DOI

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License

Creative Commons BY-NC 3.0

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12-Lead ECG Week 38 Mepolizumab HES NCT00086658

12-Lead ECG Week 38

  1. StudyEvent: ODM
    1. 12-Lead ECG Week 38
12-Lead ECG
Description

12-Lead ECG

Alias
UMLS CUI-1
C0430456
Subject ID
Description

Subject ID

Data type

text

Alias
UMLS CUI [1]
C2348585
Visit Date
Description

Visit Date

Data type

date

Alias
UMLS CUI [1]
C1320303
Date of ECG
Description

Date of ECG

Data type

date

Alias
UMLS CUI [1]
C2826640
Result of the ECG
Description

Result of the ECG

Data type

text

Alias
UMLS CUI [1]
C0438154

Similar models

12-Lead ECG Week 38

  1. StudyEvent: ODM
    1. 12-Lead ECG Week 38
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
12-Lead ECG
C0430456 (UMLS CUI-1)
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Date of ECG
Item
Date of ECG
date
C2826640 (UMLS CUI [1])
Item
Result of the ECG
text
C0438154 (UMLS CUI [1])
Code List
Result of the ECG
CL Item
Clinically significant change from Baseline favourable (Clinically significant change from Baseline favourable)
CL Item
Clinically significant change from Baseline unfavourable (Clinically significant change from Baseline unfavourable)
CL Item
No change or insignificant change from Baseline (No change or insignificant change from Baseline)
CL Item
No result (not available (No result (not available)

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