Information:
Fel:
ID
32696
Beskrivning
A Study to Compare the Safety and Drug Levels in Blood When Using Various Forms of GSK189075 Given to Healthy Subjects; ODM derived from: https://clinicaltrials.gov/show/NCT00559884
Länk
https://clinicaltrials.gov/show/NCT00559884
Nyckelord
Versioner (1)
- 2018-11-12 2018-11-12 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
12 november 2018
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 Type 2 Diabetes Mellitus NCT00559884
Eligibility Type 2 Diabetes Mellitus NCT00559884
- StudyEvent: Eligibility
Similar models
Eligibility Type 2 Diabetes Mellitus NCT00559884
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Healthy adult | Non-smoker | Age
Item
are a healthy, non-smoking adult, 18 to 55 years old.
boolean
C0686750 (UMLS CUI [1])
C0337672 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
C0337672 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
Normal body weight
Item
are not overly thin or overly heavy for your height.
boolean
C1285592 (UMLS CUI [1])
Female infertility | Gender Contraceptive methods
Item
are a female who is unable to have children, or is willing to use birth control throughout the study.
boolean
C0021361 (UMLS CUI [1])
C0079399 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0079399 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
Protocol Compliance | Informed Consent
Item
are willing and able to follow all study-related instructions provided by the site staff. - are willing to provide signed consent.
boolean
C0525058 (UMLS CUI [1])
C0021430 (UMLS CUI [2])
C0021430 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
are a pregnant or a nursing female.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Heart Disease | Liver disease | Kidney Disease | Hematological Disease | Brain Disease | Disease Other
Item
have a past or current disease such as heart, liver, kidney, blood, brain, or other disease.
boolean
C0018799 (UMLS CUI [1])
C0023895 (UMLS CUI [2])
C0022658 (UMLS CUI [3])
C0018939 (UMLS CUI [4])
C0006111 (UMLS CUI [5])
C0012634 (UMLS CUI [6,1])
C0205394 (UMLS CUI [6,2])
C0023895 (UMLS CUI [2])
C0022658 (UMLS CUI [3])
C0018939 (UMLS CUI [4])
C0006111 (UMLS CUI [5])
C0012634 (UMLS CUI [6,1])
C0205394 (UMLS CUI [6,2])
Communicable Diseases
Item
have had certain infections within 4 weeks before the expected the first dose of study drug.
boolean
C0009450 (UMLS CUI [1])
HIV Infection | Hepatitis | Alcohol intake Screening
Item
have hiv or hepatitis, or have alcohol in your system at the screening visit.
boolean
C0019693 (UMLS CUI [1])
C0019158 (UMLS CUI [2])
C0001948 (UMLS CUI [3,1])
C1710477 (UMLS CUI [3,2])
C0019158 (UMLS CUI [2])
C0001948 (UMLS CUI [3,1])
C1710477 (UMLS CUI [3,2])
Alcohol abuse
Item
have a history of alcohol abuse.
boolean
C0085762 (UMLS CUI [1])
Study Subject Participation Status | Investigational New Drugs
Item
have been in another research study in the last month or have taken certain medications in the 2 weeks before study drug would be taken.
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C0013230 (UMLS CUI [2])
Laboratory test result abnormal
Item
have laboratory tests that are outside the normal range.
boolean
C0438215 (UMLS CUI [1])