ID

33112

Descripción

A Clinical Study to Evaluate the Effect of Naturlose (Tagatose); ODM derived from: https://clinicaltrials.gov/show/NCT00961662

Link

https://clinicaltrials.gov/show/NCT00961662

Palabras clave

Versiones (1)
  1. 28/11/18 28/11/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

28 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 NCT00961662

Inglés

Eligibility Type 2 Diabetes NCT00961662

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
type 2 diabetics in accordance with who.
Descripción

Non-Insulin-Dependent Diabetes Mellitus WHO classification

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0011860
UMLS CUI [1,2]
C4267671
male and female patients, between 18 and 75 years of age.
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
diabetic patients who are not on medication for the disease. patients may be treated with diet and exercise.
Descripción

Diabetic | Pharmaceutical Preparations Absent | Diet therapy | Exercise

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0241863
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C0332197
UMLS CUI [3]
C0012159
UMLS CUI [4]
C0015259
normal blood creatine clearance and normal liver function test results.
Descripción

Creatinine clearance Normal | Liver function tests normal

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0812399
UMLS CUI [1,2]
C0205307
UMLS CUI [2]
C0438235
bmi less than or equal to 45 kg/m2
Descripción

Body mass index

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1305855
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
treatment with sulfonylurea (e.g., glyburide, glipizide, glimepiride, chlorpropamide, tolazamide, acetohexamide, or tolbutamide), tzds, metformin, acarbose, byetta, insulin, and any antidiabetic medications within the prior 3 months.
Descripción

Sulfonylurea | Glyburide | Glipizide | glimepiride | Chlorpropamide | Tolazamide | Acetohexamide | Tolbutamide | Thiazolidinediones | Metformin | Acarbose | Byetta | Insulin | Antidiabetics

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0038766
UMLS CUI [2]
C0017628
UMLS CUI [3]
C0017642
UMLS CUI [4]
C0061323
UMLS CUI [5]
C0008287
UMLS CUI [6]
C0040372
UMLS CUI [7]
C0000992
UMLS CUI [8]
C0040374
UMLS CUI [9]
C1257987
UMLS CUI [10]
C0025598
UMLS CUI [11]
C0050393
UMLS CUI [12]
C1636686
UMLS CUI [13]
C0021641
UMLS CUI [14]
C0935929
therapy with beta-blockers or thiazide diuretics within the prior 3 months
Descripción

Adrenergic beta-1 Receptor Antagonists | Thiazide Diuretics

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0304516
UMLS CUI [2]
C0012802
pregnancy, breastfeeding, or intention of becoming pregnant or judged to be using inadequate contraceptive measure.
Descripción

Pregnancy | Breast Feeding | Pregnancy, Planned | Contraceptive methods Inadequate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992
UMLS CUI [4,1]
C0700589
UMLS CUI [4,2]
C0205412
documented gastrointestinal disease, or taking of medications likely to alter gut motility or absorption.
Descripción

Gastrointestinal Disease | Pharmaceutical Preparations Changing Gastrointestinal Motility | Pharmaceutical Preparations Changing Gastrointestinal Absorption

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0017178
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C0392747
UMLS CUI [2,3]
C0017184
UMLS CUI [3,1]
C0013227
UMLS CUI [3,2]
C0392747
UMLS CUI [3,3]
C3714657
receiving any investigational drug within 30 days of the baseline visit.
Descripción

Investigational New Drugs

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0013230
Volver a la parte superior de la página

Similar models

Eligibility Type 2 Diabetes NCT00961662

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Non-Insulin-Dependent Diabetes Mellitus WHO classification
Item
type 2 diabetics in accordance with who.
boolean
C0011860 (UMLS CUI [1,1])
C4267671 (UMLS CUI [1,2])
Age
Item
male and female patients, between 18 and 75 years of age.
boolean
C0001779 (UMLS CUI [1])
Diabetic | Pharmaceutical Preparations Absent | Diet therapy | Exercise
Item
diabetic patients who are not on medication for the disease. patients may be treated with diet and exercise.
boolean
C0241863 (UMLS CUI [1])
C0013227 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0012159 (UMLS CUI [3])
C0015259 (UMLS CUI [4])
Creatinine clearance Normal | Liver function tests normal
Item
normal blood creatine clearance and normal liver function test results.
boolean
C0812399 (UMLS CUI [1,1])
C0205307 (UMLS CUI [1,2])
C0438235 (UMLS CUI [2])
Body mass index
Item
bmi less than or equal to 45 kg/m2
boolean
C1305855 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Sulfonylurea | Glyburide | Glipizide | glimepiride | Chlorpropamide | Tolazamide | Acetohexamide | Tolbutamide | Thiazolidinediones | Metformin | Acarbose | Byetta | Insulin | Antidiabetics
Item
treatment with sulfonylurea (e.g., glyburide, glipizide, glimepiride, chlorpropamide, tolazamide, acetohexamide, or tolbutamide), tzds, metformin, acarbose, byetta, insulin, and any antidiabetic medications within the prior 3 months.
boolean
C0038766 (UMLS CUI [1])
C0017628 (UMLS CUI [2])
C0017642 (UMLS CUI [3])
C0061323 (UMLS CUI [4])
C0008287 (UMLS CUI [5])
C0040372 (UMLS CUI [6])
C0000992 (UMLS CUI [7])
C0040374 (UMLS CUI [8])
C1257987 (UMLS CUI [9])
C0025598 (UMLS CUI [10])
C0050393 (UMLS CUI [11])
C1636686 (UMLS CUI [12])
C0021641 (UMLS CUI [13])
C0935929 (UMLS CUI [14])
Adrenergic beta-1 Receptor Antagonists | Thiazide Diuretics
Item
therapy with beta-blockers or thiazide diuretics within the prior 3 months
boolean
C0304516 (UMLS CUI [1])
C0012802 (UMLS CUI [2])
Pregnancy | Breast Feeding | Pregnancy, Planned | Contraceptive methods Inadequate
Item
pregnancy, breastfeeding, or intention of becoming pregnant or judged to be using inadequate contraceptive measure.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
C0700589 (UMLS CUI [4,1])
C0205412 (UMLS CUI [4,2])
Gastrointestinal Disease | Pharmaceutical Preparations Changing Gastrointestinal Motility | Pharmaceutical Preparations Changing Gastrointestinal Absorption
Item
documented gastrointestinal disease, or taking of medications likely to alter gut motility or absorption.
boolean
C0017178 (UMLS CUI [1])
C0013227 (UMLS CUI [2,1])
C0392747 (UMLS CUI [2,2])
C0017184 (UMLS CUI [2,3])
C0013227 (UMLS CUI [3,1])
C0392747 (UMLS CUI [3,2])
C3714657 (UMLS CUI [3,3])
Investigational New Drugs
Item
receiving any investigational drug within 30 days of the baseline visit.
boolean
C0013230 (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