ID

15494

Beschreibung

The DREAM (Diabetes Reduction Assessment With Ramipril and Rosiglitazone Medication) Trial; ODM derived from: https://clinicaltrials.gov/show/NCT00095654

Link

https://clinicaltrials.gov/show/NCT00095654

Stichworte

Versionen (1)
  1. 01.06.16 01.06.16 -
Hochgeladen am

1. Juni 2016

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Impaired Glucose Tolerance NCT00095654

Englisch

Eligibility Impaired Glucose Tolerance NCT00095654

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
impaired glucose tolerance (fpg < 7 mmol/l or 126 mg/dl and 2 hr pg >= 7.8 mmol/l and < 11.1 mmol/l (140 mg/dl and < 200 mg/dl)or,
Beschreibung

glucose tolerance

Datentyp

boolean

Alias
UMLS CUI [1]
C0271650
isolated impaired fasting glucose (fpg >= 6.1 mmol/l and < 7 mmol/l (fpg >= 95 mg/dl and < 126 mg/dl) and 2 hr pg < 7.8 mmol/l (140 mg/dl).
Beschreibung

impaired fasting glucose

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1272092
UMLS CUI [1,2]
C0205409
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
current use of an ace-inhibitor (ace-i) or thiazolidinedione(tzd)
Beschreibung

ace-inhibitor or thiazolidinedione

Datentyp

boolean

Alias
UMLS CUI [1]
C0003015
UMLS CUI [2]
C1257987
known hypersensitivity to ace-i
Beschreibung

hypersensitivity to ace-i

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0003015
prior use of anti-diabetic medications (with the exception of during pregnancy)
Beschreibung

anti-diabetic medications

Datentyp

boolean

Alias
UMLS CUI [1]
C0935929
use of systemic glucocorticoids or niacin
Beschreibung

systemic glucocorticoids or niacin

Datentyp

boolean

Alias
UMLS CUI [1]
C3540777
UMLS CUI [2]
C0027996
congestive heart failure or ef < 40%
Beschreibung

congestive heart failure

Datentyp

boolean

Alias
UMLS CUI [1]
C0018802
UMLS CUI [2]
C0232174
existing cardiovascular disease (previous mi, stroke, angina, uncontrolled hypertension)
Beschreibung

existing cardiovascular disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0038454
UMLS CUI [3]
C0002962
UMLS CUI [4]
C1868885
diabetes
Beschreibung

diabetes

Datentyp

boolean

Alias
UMLS CUI [1]
C0011849
renal or hepatic disease
Beschreibung

renal or hepatic disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0023895
UMLS CUI [2]
C0022658
major illness
Beschreibung

major illness

Datentyp

boolean

Alias
UMLS CUI [1]
C0009488
use of another experimental drug
Beschreibung

another experimental drug

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
pregnant or unwilling to use reliable contraception
Beschreibung

pregnant or unwilling contraception

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C1999124
major psychiatric disorder
Beschreibung

major psychiatric disorder

Datentyp

boolean

Alias
UMLS CUI [1]
C0004936
diseases that affect glucose tolerance
Beschreibung

diseases that affect glucose tolerance

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0178665
unwillingness to be randomized or sign informed consent
Beschreibung

informed consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
known uncontrolled substance abuse
Beschreibung

substance abuse

Datentyp

boolean

Alias
UMLS CUI [1]
C0038586
inability to communicate with research staff
Beschreibung

inability to communicate

Datentyp

boolean

Alias
UMLS CUI [1]
C1145677
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Ähnliche Modelle

Eligibility Impaired Glucose Tolerance NCT00095654

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
glucose tolerance
Item
impaired glucose tolerance (fpg < 7 mmol/l or 126 mg/dl and 2 hr pg >= 7.8 mmol/l and < 11.1 mmol/l (140 mg/dl and < 200 mg/dl)or,
boolean
C0271650 (UMLS CUI [1])
impaired fasting glucose
Item
isolated impaired fasting glucose (fpg >= 6.1 mmol/l and < 7 mmol/l (fpg >= 95 mg/dl and < 126 mg/dl) and 2 hr pg < 7.8 mmol/l (140 mg/dl).
boolean
C1272092 (UMLS CUI [1,1])
C0205409 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
ace-inhibitor or thiazolidinedione
Item
current use of an ace-inhibitor (ace-i) or thiazolidinedione(tzd)
boolean
C0003015 (UMLS CUI [1])
C1257987 (UMLS CUI [2])
hypersensitivity to ace-i
Item
known hypersensitivity to ace-i
boolean
C0020517 (UMLS CUI [1,1])
C0003015 (UMLS CUI [1,2])
anti-diabetic medications
Item
prior use of anti-diabetic medications (with the exception of during pregnancy)
boolean
C0935929 (UMLS CUI [1])
systemic glucocorticoids or niacin
Item
use of systemic glucocorticoids or niacin
boolean
C3540777 (UMLS CUI [1])
C0027996 (UMLS CUI [2])
congestive heart failure
Item
congestive heart failure or ef < 40%
boolean
C0018802 (UMLS CUI [1])
C0232174 (UMLS CUI [2])
existing cardiovascular disease
Item
existing cardiovascular disease (previous mi, stroke, angina, uncontrolled hypertension)
boolean
C0027051 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0002962 (UMLS CUI [3])
C1868885 (UMLS CUI [4])
diabetes
Item
diabetes
boolean
C0011849 (UMLS CUI [1])
renal or hepatic disease
Item
renal or hepatic disease
boolean
C0023895 (UMLS CUI [1])
C0022658 (UMLS CUI [2])
major illness
Item
major illness
boolean
C0009488 (UMLS CUI [1])
another experimental drug
Item
use of another experimental drug
boolean
C2348568 (UMLS CUI [1])
pregnant or unwilling contraception
Item
pregnant or unwilling to use reliable contraception
boolean
C0032961 (UMLS CUI [1])
C1999124 (UMLS CUI [2])
major psychiatric disorder
Item
major psychiatric disorder
boolean
C0004936 (UMLS CUI [1])
diseases that affect glucose tolerance
Item
diseases that affect glucose tolerance
boolean
C0009488 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0178665 (UMLS CUI [1,3])
informed consent
Item
unwillingness to be randomized or sign informed consent
boolean
C0021430 (UMLS CUI [1])
substance abuse
Item
known uncontrolled substance abuse
boolean
C0038586 (UMLS CUI [1])
inability to communicate
Item
inability to communicate with research staff
boolean
C1145677 (UMLS CUI [1])
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