ID

34292

Beskrivning

Pharmacokinetics, Safety and Tolerability of Oral Semaglutide in Subjects With Various Degrees of Impaired Renal Function; ODM derived from: https://clinicaltrials.gov/show/NCT02014259

Länk

https://clinicaltrials.gov/show/NCT02014259

Nyckelord

  1. 2019-01-16 2019-01-16 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

16 januari 2019

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0

Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility Diabetes NCT02014259

Eligibility Diabetes NCT02014259

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT02014259
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female aged 18-85 years (both inclusive) at the time of signing inform consent
Beskrivning

ID.1

Datatyp

boolean

subject with normal renal function or renal impairment (mild, moderate, severe or end-stage renal disease requiring dialysis)
Beskrivning

ID.2

Datatyp

boolean

for subject with normal renal function: good general health (as judged by the investigator)
Beskrivning

ID.3

Datatyp

boolean

body mass index (bmi) 18.5-40.0 kg/m^2 (both inclusive)
Beskrivning

ID.4

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using adequate contraceptive methods
Beskrivning

ID.5

Datatyp

boolean

history of crohn's disease, ulcerative colitis, or other inflammatory bowel disease
Beskrivning

ID.6

Datatyp

boolean

uncontrolled hypertension (defined as systolic blood pressure above or equal to 180 mmhg and/or diastolic blood pressure above or equal to 100 mmhg)
Beskrivning

ID.7

Datatyp

boolean

any blood draw or donation of blood or plasma in excess of 400 ml within the 3 months preceding the screening visit (visit 2)
Beskrivning

ID.8

Datatyp

boolean

history of significant drug abuse, or a positive drug test at the screening visit (visit 2)
Beskrivning

ID.9

Datatyp

boolean

Similar models

Eligibility Diabetes NCT02014259

  1. StudyEvent: Eligibility
    1. Eligibility Diabetes NCT02014259
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
male or female aged 18-85 years (both inclusive) at the time of signing inform consent
boolean
ID.2
Item
subject with normal renal function or renal impairment (mild, moderate, severe or end-stage renal disease requiring dialysis)
boolean
ID.3
Item
for subject with normal renal function: good general health (as judged by the investigator)
boolean
ID.4
Item
body mass index (bmi) 18.5-40.0 kg/m^2 (both inclusive)
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
female who is pregnant, breast-feeding or intends to become pregnant or is of child-bearing potential and not using adequate contraceptive methods
boolean
ID.6
Item
history of crohn's disease, ulcerative colitis, or other inflammatory bowel disease
boolean
ID.7
Item
uncontrolled hypertension (defined as systolic blood pressure above or equal to 180 mmhg and/or diastolic blood pressure above or equal to 100 mmhg)
boolean
ID.8
Item
any blood draw or donation of blood or plasma in excess of 400 ml within the 3 months preceding the screening visit (visit 2)
boolean
ID.9
Item
history of significant drug abuse, or a positive drug test at the screening visit (visit 2)
boolean

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial