ID

41034

Description

Study ID: 103447 Clinical Study ID: NKV103447 Study Title:A study to evaluate the effect of casoptiant on cardiac conduction as assessed by 12-lead electrocardiogram as compared to placebo and moxifloxacin Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Phase: Phase 1 Study Recruitment Status: Completed Generic Name: casopitant Trade Name: Rezonic,Zunrisa; Zunrisa,Rezonic Study Indication: Nausea and Vomiting, Chemotherapy-Induced

Keywords

Versions (1)
  1. 15/6/20 15/6/20 -
Copyright Holder

GlaxoSmithKline

Uploaded on

15 de junio de 2020

DOI

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License

Creative Commons BY-NC 4.0
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Effect of casoptiant on cardiac conduction as compared to placebo and moxifloxacin 103447

English

Urine Pregnancy Test; Serology

1 forms  
Administrative
Description

Administrative

Alias
UMLS CUI-1
C1320722
Subject Identifier
Description

Subject Identifier

Data type

text

Alias
UMLS CUI [1]
C2348585
Urine Pregnancy Test (Complete for Female Subjects Only) (Screening, Day-1, Follow-up)
Description

Urine Pregnancy Test (Complete for Female Subjects Only) (Screening, Day-1, Follow-up)

Alias
UMLS CUI-1
C0430056
Date sample taken (Pregnancy Test)
Description

Date sample taken (Pregnancy Test)

Data type

date

Alias
UMLS CUI [1]
C1302413
UMLS CUI [2]
C0032976
Results
Description

Results

Data type

integer

Alias
UMLS CUI [1]
C1254595
Serology
Description

Serology

Alias
UMLS CUI-1
C0036743
Date sample taken (Serology)
Description

Date sample taken (Serology)

Data type

date

Alias
UMLS CUI [1]
C1302413
UMLS CUI [2]
C0036743
HIV antibody
Description

HIV antibody

Data type

integer

Alias
UMLS CUI [1]
C0019683
Hepatitis B surface antigen
Description

Hepatitis B surface antigen

Data type

integer

Alias
UMLS CUI [1]
C0019168
Hepatitis C antibody
Description

Hepatitis C antibody

Data type

integer

Alias
UMLS CUI [1]
C0201487
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Similar models

Urine Pregnancy Test; Serology

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative
C1320722 (UMLS CUI-1)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Item Group
Urine Pregnancy Test (Complete for Female Subjects Only) (Screening, Day-1, Follow-up)
C0430056 (UMLS CUI-1)
Date sample taken (Pregnancy Test)
Item
Date sample taken (Pregnancy Test)
date
C1302413 (UMLS CUI [1])
C0032976 (UMLS CUI [2])
Item
Results
integer
C1254595 (UMLS CUI [1])
Results
Code List
Results
CL Item
Positive (1)
CL Item
Negative (2)
Item Group
Serology
C0036743 (UMLS CUI-1)
Date sample taken (Serology)
Item
Date sample taken (Serology)
date
C1302413 (UMLS CUI [1])
C0036743 (UMLS CUI [2])
Item
HIV antibody
integer
C0019683 (UMLS CUI [1])
HIV antibody
Code List
HIV antibody
CL Item
Positive (1)
CL Item
Negative (2)
Item
Hepatitis B surface antigen
integer
C0019168 (UMLS CUI [1])
Hepatitis B surface antigen
Code List
Hepatitis B surface antigen
CL Item
Positive (1)
CL Item
Negative (2)
Item
Hepatitis C antibody
integer
C0201487 (UMLS CUI [1])
Hepatitis C antibody
Code List
Hepatitis C antibody
CL Item
Positive (1)
CL Item
Negative (2)
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