ID

34590

Beschreibung

Pharmacokinetic/Pharmacodynamic Drug-drug Interaction of DA-1229 and Metformin After Oral Administration in Healthy Male Subjects; ODM derived from: https://clinicaltrials.gov/show/NCT01941199

Link

https://clinicaltrials.gov/show/NCT01941199

Stichworte

  1. 19.01.19 19.01.19 -
Rechteinhaber

see on clinicaltrials.gov

Hochgeladen am

19. Januar 2019

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Type 2 Diabetes Mellitus NCT01941199

Eligibility Type 2 Diabetes Mellitus NCT01941199

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
age between 20 to 45, healthy male subjects(at screening)
Beschreibung

ID.1

Datentyp

boolean

body weight between 55kg - 90kg, bmi between 18.0 - 27.0
Beschreibung

ID.2

Datentyp

boolean

fpg 70-125mg/dl glucose level(at screening)
Beschreibung

ID.3

Datentyp

boolean

subject who totally understand the progress of this clinical trials, make decision by his free will, and signed a consent form to follow the progress.
Beschreibung

ID.4

Datentyp

boolean

Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
subject who has past or present history of any diseases following below.(liver including hepatitis virus carrier, kidney, neurology, immunology, pulmonary, endocrine, hematooncology, cardiology, mental disorder)
Beschreibung

ID.5

Datentyp

boolean

subject who had gi tract disease(crohn's disease, ulcer, acute or chronic pancreatitis) or surgery(appendectomy, hernioplasty are excluded)
Beschreibung

ID.6

Datentyp

boolean

subject who had drug(aspirin, antibiotics) hypersensitivity reaction
Beschreibung

ID.7

Datentyp

boolean

subject who already participated in other trials in 2 months
Beschreibung

ID.8

Datentyp

boolean

subject who had whole blood donation in 2 months, or component blood donation in 1 months or transfusion in 1 months currently.
Beschreibung

ID.9

Datentyp

boolean

Ähnliche Modelle

Eligibility Type 2 Diabetes Mellitus NCT01941199

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
age between 20 to 45, healthy male subjects(at screening)
boolean
ID.2
Item
body weight between 55kg - 90kg, bmi between 18.0 - 27.0
boolean
ID.3
Item
fpg 70-125mg/dl glucose level(at screening)
boolean
ID.4
Item
subject who totally understand the progress of this clinical trials, make decision by his free will, and signed a consent form to follow the progress.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
subject who has past or present history of any diseases following below.(liver including hepatitis virus carrier, kidney, neurology, immunology, pulmonary, endocrine, hematooncology, cardiology, mental disorder)
boolean
ID.6
Item
subject who had gi tract disease(crohn's disease, ulcer, acute or chronic pancreatitis) or surgery(appendectomy, hernioplasty are excluded)
boolean
ID.7
Item
subject who had drug(aspirin, antibiotics) hypersensitivity reaction
boolean
ID.8
Item
subject who already participated in other trials in 2 months
boolean
ID.9
Item
subject who had whole blood donation in 2 months, or component blood donation in 1 months or transfusion in 1 months currently.
boolean

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