ID

32867

Descripción

Shiga Progression of Diabetes, Nephropathy and Retinopathy; ODM derived from: https://clinicaltrials.gov/show/NCT00846716

Link

https://clinicaltrials.gov/show/NCT00846716

Palabras clave

Versiones (1)
  1. 17/11/18 17/11/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

17 de noviembre de 2018

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Type 2 Diabetes Mellitus NCT00846716

Inglés

Eligibility Type 2 Diabetes Mellitus NCT00846716

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetes mellitus
Descripción

Diabetes Mellitus, Non-Insulin-Dependent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011860
less than 8.0% in hba1c
Descripción

Hemoglobin A1c measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0474680
less than 300 mg/g cr of urinary albumine level
Descripción

Urine albumin/creatinine ratio measurement

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0455271
concomitant therapy with su and/or biguanide
Descripción

Sulfonylurea | Biguanide

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038766
UMLS CUI [2]
C0005382
untreated hypertension and hypertension treated with arb or acei
Descripción

Hypertensive disease Untreated | Hypertensive disease | Angiotensin II receptor antagonist | Angiotensin-Converting Enzyme Inhibitors

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0332155
UMLS CUI [2]
C0020538
UMLS CUI [3]
C0521942
UMLS CUI [4]
C0003015
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of heart failure and concomitant heart failure
Descripción

Heart failure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0018801
history of administration of tzd agent
Descripción

Thiazolidinediones

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1257987
severe hepatic dysfunction with more than 3 times higher than upper limit of normal range of got, gpt or rgpt
Descripción

Liver Dysfunction Severe | Aspartate aminotransferase increased | Alanine aminotransferase increased

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0086565
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0151904
UMLS CUI [3]
C0151905
severe renal dysfunction with more than 2.5 of cr
Descripción

Renal dysfunction Severe | Serum creatinine raised

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3279454
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0700225
history of ae with tzd agent
Descripción

Adverse events Thiazolidinediones Related

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C1257987
UMLS CUI [1,3]
C0439849
insulin treatment
Descripción

Insulin regime

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0557978
concomitant urinary track infection
Descripción

Urinary tract infection

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0042029
Volver a la parte superior de la página

Similar models

Eligibility Type 2 Diabetes Mellitus NCT00846716

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Diabetes Mellitus, Non-Insulin-Dependent
Item
type 2 diabetes mellitus
boolean
C0011860 (UMLS CUI [1])
Hemoglobin A1c measurement
Item
less than 8.0% in hba1c
boolean
C0474680 (UMLS CUI [1])
Urine albumin/creatinine ratio measurement
Item
less than 300 mg/g cr of urinary albumine level
boolean
C0455271 (UMLS CUI [1])
Sulfonylurea | Biguanide
Item
concomitant therapy with su and/or biguanide
boolean
C0038766 (UMLS CUI [1])
C0005382 (UMLS CUI [2])
Hypertensive disease Untreated | Hypertensive disease | Angiotensin II receptor antagonist | Angiotensin-Converting Enzyme Inhibitors
Item
untreated hypertension and hypertension treated with arb or acei
boolean
C0020538 (UMLS CUI [1,1])
C0332155 (UMLS CUI [1,2])
C0020538 (UMLS CUI [2])
C0521942 (UMLS CUI [3])
C0003015 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
Heart failure
Item
history of heart failure and concomitant heart failure
boolean
C0018801 (UMLS CUI [1])
Thiazolidinediones
Item
history of administration of tzd agent
boolean
C1257987 (UMLS CUI [1])
Liver Dysfunction Severe | Aspartate aminotransferase increased | Alanine aminotransferase increased
Item
severe hepatic dysfunction with more than 3 times higher than upper limit of normal range of got, gpt or rgpt
boolean
C0086565 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0151904 (UMLS CUI [2])
C0151905 (UMLS CUI [3])
Renal dysfunction Severe | Serum creatinine raised
Item
severe renal dysfunction with more than 2.5 of cr
boolean
C3279454 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0700225 (UMLS CUI [2])
Adverse events Thiazolidinediones Related
Item
history of ae with tzd agent
boolean
C0877248 (UMLS CUI [1,1])
C1257987 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
Insulin regime
Item
insulin treatment
boolean
C0557978 (UMLS CUI [1])
Urinary tract infection
Item
concomitant urinary track infection
boolean
C0042029 (UMLS CUI [1])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial