Eligibility Atrial Fibrillation NCT02390258

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
for parts 1 and 3 healthy, male subjects aged 18 to 45 years, inclusive. for part 2 healthy, male and female subjects aged 45 to 65 years, inclusive.
Descrição

ID.1

Tipo de dados

boolean

females must be of non-childbearing potential
Descrição

ID.2

Tipo de dados

boolean

Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
subject has a known heart disease.
Descrição

ID.3

Tipo de dados

boolean

subject has any of qtcf > 450 msec, pr ≥ 210 msec or qrs ≥ 120 msec at screening (determined from median of three readings).
Descrição

ID.4

Tipo de dados

boolean

for part 1 only: subject has resting heart rate outside of the range 45 to 80 beats per minute (bpm) at screening (determined from median of three readings).
Descrição

ID.5

Tipo de dados

boolean

subject has any other condition which, in the investigator's opinion will interfere with the trial.
Descrição

ID.6

Tipo de dados

boolean

subject has a systolic blood pressure (bp) <80 or >160 mmhg at screening or a diastolic bp >90 or <45 mmhg at screening.
Descrição

ID.7

Tipo de dados

boolean

subject has a clinically significant abnormal laboratory test result at screening.
Descrição

ID.8

Tipo de dados

boolean

female subject who is pregnant or breast feeding and female subjects of childbearing potential.
Descrição

ID.9

Tipo de dados

boolean

Similar models

Eligibility Atrial Fibrillation NCT02390258

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
for parts 1 and 3 healthy, male subjects aged 18 to 45 years, inclusive. for part 2 healthy, male and female subjects aged 45 to 65 years, inclusive.
boolean
ID.2
Item
females must be of non-childbearing potential
boolean
Item Group
C0680251 (UMLS CUI)
ID.3
Item
subject has a known heart disease.
boolean
ID.4
Item
subject has any of qtcf > 450 msec, pr ≥ 210 msec or qrs ≥ 120 msec at screening (determined from median of three readings).
boolean
ID.5
Item
for part 1 only: subject has resting heart rate outside of the range 45 to 80 beats per minute (bpm) at screening (determined from median of three readings).
boolean
ID.6
Item
subject has any other condition which, in the investigator's opinion will interfere with the trial.
boolean
ID.7
Item
subject has a systolic blood pressure (bp) <80 or >160 mmhg at screening or a diastolic bp >90 or <45 mmhg at screening.
boolean
ID.8
Item
subject has a clinically significant abnormal laboratory test result at screening.
boolean
ID.9
Item
female subject who is pregnant or breast feeding and female subjects of childbearing potential.
boolean