ID

38744

Descripción

Single Oral Dose of BeneFlax to Healthy Young and Older Adults; ODM derived from: https://clinicaltrials.gov/show/NCT01531569

Link

https://clinicaltrials.gov/show/NCT01531569

Palabras clave

Versiones (1)
  1. 31/10/19 31/10/19 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

31 de octubre de 2019

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 Diabetes Mellitus, Type 2 NCT01531569

Inglés

Eligibility Diabetes Mellitus, Type 2 NCT01531569

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
healthy adults: 18-45 and 60-80 years of age
Descripción

Well adult | Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0686750
UMLS CUI [2]
C0001779
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
strict vegetarians and vegans (as these diets likely contain foods which have higher levels of lignans)
Descripción

Strict vegetarian | Vegan | Lignans High Level

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3241968
UMLS CUI [2]
C2987738
UMLS CUI [3,1]
C0064971
UMLS CUI [3,2]
C4321237
strict vegetarians and vegans (as these diets likely contain foods which have higher levels of lignans)
Descripción

Strict vegetarian | Vegan | Lignans High Level

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3241968
UMLS CUI [2]
C2987738
UMLS CUI [3,1]
C0064971
UMLS CUI [3,2]
C4321237
individuals who smoke
Descripción

Tobacco use

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0543414
individuals who have experienced diarrhea in the last three months
Descripción

Diarrhea

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011991
individuals who have taken oral antibiotics in the last three months
Descripción

Antidiabetics Oral

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0935929
UMLS CUI [1,2]
C1527415
individuals who are currently taking warfarin or any of its derivatives
Descripción

Warfarin | Warfarin Derivative

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0043031
UMLS CUI [2,1]
C0043031
UMLS CUI [2,2]
C1527240
individuals with low haemoglobin (<121g/l for women and <137g/l for men)
Descripción

Hemoglobin low | Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0162119
UMLS CUI [2]
C0079399
individuals with bmi under 19 or over 28
Descripción

Body mass index

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1305855
pregnant or lactating women
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
women with child bearing potential not using contraceptives
Descripción

Childbearing Potential Contraceptive methods Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
UMLS CUI [1,3]
C0332197
current diagnosis of a bleeding disorder or at risk of bleeding
Descripción

Blood Coagulation Disorder | Bleeding risk

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005779
UMLS CUI [2]
C3251812
individuals with gastrointestinal problems (such as ulcers), or convulsive, depressive, or hepatic disorders
Descripción

Gastrointestinal problem | Ulcers | Convulsive disorder | Depressive disorder | Liver diseases

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0017187
UMLS CUI [2]
C0041582
UMLS CUI [3]
C0234972
UMLS CUI [4]
C0011581
UMLS CUI [5]
C0023895
individuals with diabetes mellitus
Descripción

Diabetes Mellitus

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011849
individuals currently taking a flax seed supplement
Descripción

Flaxseed Supplement

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0995001
UMLS CUI [1,2]
C0242295
individuals with an allergy to flax seed
Descripción

Hypersensitivity Flaxseed

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0995001
individuals who have donated blood or lost > 450 ml of blood within 56 days of study duration
Descripción

Blood Donation Amount Timespan | Blood Loss Amount Timespan

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0005794
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0872291
UMLS CUI [2,1]
C3163616
UMLS CUI [2,2]
C1265611
UMLS CUI [2,3]
C0872291
individuals who have participated in any other clinical trial with and investigational agent within one month of starting this trial
Descripción

Study Subject Participation Status | Investigational New Drugs

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
Volver a la parte superior de la página

Similar models

Eligibility Diabetes Mellitus, Type 2 NCT01531569

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Well adult | Age
Item
healthy adults: 18-45 and 60-80 years of age
boolean
C0686750 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Strict vegetarian | Vegan | Lignans High Level
Item
strict vegetarians and vegans (as these diets likely contain foods which have higher levels of lignans)
boolean
C3241968 (UMLS CUI [1])
C2987738 (UMLS CUI [2])
C0064971 (UMLS CUI [3,1])
C4321237 (UMLS CUI [3,2])
Strict vegetarian | Vegan | Lignans High Level
Item
strict vegetarians and vegans (as these diets likely contain foods which have higher levels of lignans)
boolean
C3241968 (UMLS CUI [1])
C2987738 (UMLS CUI [2])
C0064971 (UMLS CUI [3,1])
C4321237 (UMLS CUI [3,2])
Tobacco use
Item
individuals who smoke
boolean
C0543414 (UMLS CUI [1])
Diarrhea
Item
individuals who have experienced diarrhea in the last three months
boolean
C0011991 (UMLS CUI [1])
Antidiabetics Oral
Item
individuals who have taken oral antibiotics in the last three months
boolean
C0935929 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
Warfarin | Warfarin Derivative
Item
individuals who are currently taking warfarin or any of its derivatives
boolean
C0043031 (UMLS CUI [1])
C0043031 (UMLS CUI [2,1])
C1527240 (UMLS CUI [2,2])
Hemoglobin low | Gender
Item
individuals with low haemoglobin (<121g/l for women and <137g/l for men)
boolean
C0162119 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
Body mass index
Item
individuals with bmi under 19 or over 28
boolean
C1305855 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Childbearing Potential Contraceptive methods Absent
Item
women with child bearing potential not using contraceptives
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Blood Coagulation Disorder | Bleeding risk
Item
current diagnosis of a bleeding disorder or at risk of bleeding
boolean
C0005779 (UMLS CUI [1])
C3251812 (UMLS CUI [2])
Gastrointestinal problem | Ulcers | Convulsive disorder | Depressive disorder | Liver diseases
Item
individuals with gastrointestinal problems (such as ulcers), or convulsive, depressive, or hepatic disorders
boolean
C0017187 (UMLS CUI [1])
C0041582 (UMLS CUI [2])
C0234972 (UMLS CUI [3])
C0011581 (UMLS CUI [4])
C0023895 (UMLS CUI [5])
Diabetes Mellitus
Item
individuals with diabetes mellitus
boolean
C0011849 (UMLS CUI [1])
Flaxseed Supplement
Item
individuals currently taking a flax seed supplement
boolean
C0995001 (UMLS CUI [1,1])
C0242295 (UMLS CUI [1,2])
Hypersensitivity Flaxseed
Item
individuals with an allergy to flax seed
boolean
C0020517 (UMLS CUI [1,1])
C0995001 (UMLS CUI [1,2])
Blood Donation Amount Timespan | Blood Loss Amount Timespan
Item
individuals who have donated blood or lost > 450 ml of blood within 56 days of study duration
boolean
C0005794 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0872291 (UMLS CUI [1,3])
C3163616 (UMLS CUI [2,1])
C1265611 (UMLS CUI [2,2])
C0872291 (UMLS CUI [2,3])
Study Subject Participation Status | Investigational New Drugs
Item
individuals who have participated in any other clinical trial with and investigational agent within one month of starting this trial
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
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