ID

15114

Descripción

Effect of Metformin Versus Repaglinide Treatment in Non-Obese Type 2 Diabetic Patients Uncontrolled by Diet; ODM derived from: https://clinicaltrials.gov/show/NCT00118950

Link

https://clinicaltrials.gov/show/NCT00118950

Palabras clave

  1. 16/5/16 16/5/16 -
Subido en

16 de mayo de 2016

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Diabetes Mellitus, Type 2 NCT00118950

Eligibility Diabetes Mellitus, Type 2 NCT00118950

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
type-2 diabetes, defined as:
Descripción

diabetes type 2

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0011849
UMLS CUI [1,2]
C0441730
age at onset of diabetes ≥ 40 years
Descripción

age at onset

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0001779
UMLS CUI [1,2]
C0332162
fasting serum c-peptide ≥ 300 pmol/l or a non-fasting or glucagon-stimulated serum c-peptide ≥ 600 pmol/l
Descripción

serum c-peptide

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0006558
no history of ketonuria or ketoacidosis .
Descripción

ketonuria or ketoacidosis

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0162275
UMLS CUI [1,2]
C0011880
bmi ≤ 27 kg/m2.
Descripción

bmi

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1305855
fasting plasma-glucose ≥ 6.5 mmol/l after at least one month of diet-only treatment.
Descripción

plasma-glucose

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0202042
hba1c ≤ 9.5% at ongoing oral anti-hyperglycaemic agents. hba1c ≥ 6.5% after minimum one month of diet-only treatment.
Descripción

hba1c

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019018
weight-loss of no more than 5.0 kg during the last 6 months prior to enrolment.
Descripción

weight-loss

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1262477
UMLS CUI [1,2]
C0439792
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
type-1 diabetes
Descripción

diabetes type 1

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0011849
UMLS CUI [1,2]
C0441729
insulin-treated type-2 diabetes
Descripción

diabetes type

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0011849
UMLS CUI [1,2]
C0441730
UMLS CUI [1,3]
C0745343
secondary diabetes, heart-failure
Descripción

diabetes

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0011849
UMLS CUI [1,2]
C0277555
UMLS CUI [1,3]
C0018801
serum-creatinine above the upper limit
Descripción

creatinine

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0201976
serum-asat elevated more than 3 fold above the upper limit
Descripción

asat

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0201899
factor ii-vii-x decreased below 0.7
Descripción

blood coagulating factor

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0005789
UMLS CUI [1,2]
C0547047
ongoing coexisting illnesses with a life-shortening prognosis
Descripción

life shortening comorbidity

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0023671
mental retardation or reduced intellectual behaviour
Descripción

mental retardation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0025362
pregnancy
Descripción

pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
history of drug-abuse or hba1c>10.5% at two separate visits with at least one month interval during treatment-periods.
Descripción

drug-abuse

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013146
UMLS CUI [2]
C0019018

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT00118950

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
diabetes type 2
Item
type-2 diabetes, defined as:
boolean
C0011849 (UMLS CUI [1,1])
C0441730 (UMLS CUI [1,2])
age at onset
Item
age at onset of diabetes ≥ 40 years
boolean
C0001779 (UMLS CUI [1,1])
C0332162 (UMLS CUI [1,2])
serum c-peptide
Item
fasting serum c-peptide ≥ 300 pmol/l or a non-fasting or glucagon-stimulated serum c-peptide ≥ 600 pmol/l
boolean
C0006558 (UMLS CUI [1])
ketonuria or ketoacidosis
Item
no history of ketonuria or ketoacidosis .
boolean
C0162275 (UMLS CUI [1,1])
C0011880 (UMLS CUI [1,2])
bmi
Item
bmi ≤ 27 kg/m2.
boolean
C1305855 (UMLS CUI [1])
plasma-glucose
Item
fasting plasma-glucose ≥ 6.5 mmol/l after at least one month of diet-only treatment.
boolean
C0202042 (UMLS CUI [1])
hba1c
Item
hba1c ≤ 9.5% at ongoing oral anti-hyperglycaemic agents. hba1c ≥ 6.5% after minimum one month of diet-only treatment.
boolean
C0019018 (UMLS CUI [1])
weight-loss
Item
weight-loss of no more than 5.0 kg during the last 6 months prior to enrolment.
boolean
C1262477 (UMLS CUI [1,1])
C0439792 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
diabetes type 1
Item
type-1 diabetes
boolean
C0011849 (UMLS CUI [1,1])
C0441729 (UMLS CUI [1,2])
diabetes type
Item
insulin-treated type-2 diabetes
boolean
C0011849 (UMLS CUI [1,1])
C0441730 (UMLS CUI [1,2])
C0745343 (UMLS CUI [1,3])
diabetes
Item
secondary diabetes, heart-failure
boolean
C0011849 (UMLS CUI [1,1])
C0277555 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])
creatinine
Item
serum-creatinine above the upper limit
boolean
C0201976 (UMLS CUI [1])
asat
Item
serum-asat elevated more than 3 fold above the upper limit
boolean
C0201899 (UMLS CUI [1])
blood coagulating factor
Item
factor ii-vii-x decreased below 0.7
boolean
C0005789 (UMLS CUI [1,1])
C0547047 (UMLS CUI [1,2])
life shortening comorbidity
Item
ongoing coexisting illnesses with a life-shortening prognosis
boolean
C0009488 (UMLS CUI [1,1])
C0023671 (UMLS CUI [1,2])
mental retardation
Item
mental retardation or reduced intellectual behaviour
boolean
C0025362 (UMLS CUI [1])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
drug-abuse
Item
history of drug-abuse or hba1c>10.5% at two separate visits with at least one month interval during treatment-periods.
boolean
C0013146 (UMLS CUI [1])
C0019018 (UMLS CUI [2])

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