ID

29138

Descripción

Assessment of Insulin Glargine in Type 2 Patients for Good Glycemic Control; ODM derived from: https://clinicaltrials.gov/show/NCT00701831

Link

https://clinicaltrials.gov/show/NCT00701831

Palabras clave

Versiones (1)
  1. 28/2/18 28/2/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

28 de febrero de 2018

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Diabetes Mellitus, Type 2 NCT00701831

Inglés

Eligibility Diabetes Mellitus, Type 2 NCT00701831

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
t2 insulin naïve patients
Descripción

Diabetes Mellitus, Non-Insulin-Dependent | Insulin naive

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011860
UMLS CUI [2,1]
C0021641
UMLS CUI [2,2]
C0919936
patients whom their physician is considering initiation of lantus treatment
Descripción

Lantus Initiation considering

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0876064
UMLS CUI [1,2]
C1704686
UMLS CUI [1,3]
C0750591
poor glycemic control 7,5 %10 %
Descripción

Poor glycemic control Percentage

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0342299
UMLS CUI [1,2]
C0439165
t2 treatment with oads more than 3 months
Descripción

Therapeutic procedure Non-Insulin-Dependent Diabetes Mellitus | Antidiabetics Oral

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0011860
UMLS CUI [2,1]
C0935929
UMLS CUI [2,2]
C1527415
bmi<40 kg/m2
Descripción

Body mass index

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1305855
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
impaired renal function (cr>2mg/dl or current renal dialysis)
Descripción

Renal Insufficiency | Creatinine measurement, serum | Dialysis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1565489
UMLS CUI [2]
C0201976
UMLS CUI [3]
C0011946
acute or chronic metabolic acidosis
Descripción

Metabolic acidosis | Chronic metabolic acidosis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0220981
UMLS CUI [2]
C0740749
active liver disease or serum alt or ast >2,5 than normal
Descripción

Liver disease | Alanine aminotransferase increased | Aspartate aminotransferase increased

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023895
UMLS CUI [2]
C0151905
UMLS CUI [3]
C0151904
history of hypoglycemia unawareness
Descripción

Loss of hypoglycemic warning

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0342317
diabetic retinopathy with surgery in the previous 3 months or planned within 3 months after study entry
Descripción

Diabetic Retinopathy | Operative Surgical Procedures | Operative Surgical Procedures Planned

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011884
UMLS CUI [2]
C0543467
UMLS CUI [3,1]
C0543467
UMLS CUI [3,2]
C1301732
pregnancy, breast feeding
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
Descripción

Study Subject Participation Status Aspect Additional

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1879746
UMLS CUI [1,3]
C1524062
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Similar models

Eligibility Diabetes Mellitus, Type 2 NCT00701831

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent | Insulin naive
Item
t2 insulin naïve patients
boolean
C0011860 (UMLS CUI [1])
C0021641 (UMLS CUI [2,1])
C0919936 (UMLS CUI [2,2])
Lantus Initiation considering
Item
patients whom their physician is considering initiation of lantus treatment
boolean
C0876064 (UMLS CUI [1,1])
C1704686 (UMLS CUI [1,2])
C0750591 (UMLS CUI [1,3])
Poor glycemic control Percentage
Item
poor glycemic control 7,5 %10 %
boolean
C0342299 (UMLS CUI [1,1])
C0439165 (UMLS CUI [1,2])
Therapeutic procedure Non-Insulin-Dependent Diabetes Mellitus | Antidiabetics Oral
Item
t2 treatment with oads more than 3 months
boolean
C0087111 (UMLS CUI [1,1])
C0011860 (UMLS CUI [1,2])
C0935929 (UMLS CUI [2,1])
C1527415 (UMLS CUI [2,2])
Body mass index
Item
bmi<40 kg/m2
boolean
C1305855 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Renal Insufficiency | Creatinine measurement, serum | Dialysis
Item
impaired renal function (cr>2mg/dl or current renal dialysis)
boolean
C1565489 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C0011946 (UMLS CUI [3])
Metabolic acidosis | Chronic metabolic acidosis
Item
acute or chronic metabolic acidosis
boolean
C0220981 (UMLS CUI [1])
C0740749 (UMLS CUI [2])
Liver disease | Alanine aminotransferase increased | Aspartate aminotransferase increased
Item
active liver disease or serum alt or ast >2,5 than normal
boolean
C0023895 (UMLS CUI [1])
C0151905 (UMLS CUI [2])
C0151904 (UMLS CUI [3])
Loss of hypoglycemic warning
Item
history of hypoglycemia unawareness
boolean
C0342317 (UMLS CUI [1])
Diabetic Retinopathy | Operative Surgical Procedures | Operative Surgical Procedures Planned
Item
diabetic retinopathy with surgery in the previous 3 months or planned within 3 months after study entry
boolean
C0011884 (UMLS CUI [1])
C0543467 (UMLS CUI [2])
C0543467 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
Pregnancy | Breast Feeding
Item
pregnancy, breast feeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status Aspect Additional
Item
the above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
boolean
C2348568 (UMLS CUI [1,1])
C1879746 (UMLS CUI [1,2])
C1524062 (UMLS CUI [1,3])
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