ID

29974

Descripción

Trial Comparing Metabolic Effects of Telmisartan and Amlodipine on Hypertensive Patients With Obesity and Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT00847262

Link

https://clinicaltrials.gov/show/NCT00847262

Palabras clave

Versiones (1)
  1. 2/5/18 2/5/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

2 de mayo 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 Hypertension NCT00847262

Inglés

Eligibility Hypertension NCT00847262

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
information consent signed
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
aged 30~70 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
for whom without anti-hypertensive therapy in 2 weeks：140mmhg≤sbp＜180mmhg，或90mmhg≤dbp＜110mmhg. for whom with anti-hypertensive therapies in 2 weeks：sbp＜180mmhg, 且dbp＜110mmhg
Descripción

Antihypertensive therapy Absent | Antihypertensive therapy | Systolic Pressure | Diastolic blood pressure

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0585941
UMLS CUI [1,2]
C0332197
UMLS CUI [2]
C0585941
UMLS CUI [3]
C0871470
UMLS CUI [4]
C0428883
waist circumference higher than 90cm in men, 80cm in women
Descripción

Waist Circumference | Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0455829
UMLS CUI [2]
C0079399
diagnosed diabetes
Descripción

Diabetes Mellitus

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011849
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
grade 3 hypertension: sbp≥180mmhg, or dbp≥110mmhg
Descripción

Hypertensive disease CTCAE Grades | Systolic Pressure | Diastolic blood pressure

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C1516728
UMLS CUI [2]
C0871470
UMLS CUI [3]
C0428883
waist circumference less than 90cm in men, 80cm in women
Descripción

Waist Circumference | Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0455829
UMLS CUI [2]
C0079399
known allergy or hypersensitivity to trial drugs
Descripción

Hypersensitivity Investigational New Drugs

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230
nyha grade ⅱ~ⅳ heart failure, myocardial infarction or cerebrovascular accident in 1 year preceding the trial
Descripción

Heart failure New York Heart Association Classification | Myocardial Infarction | Cerebrovascular accident

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
UMLS CUI [2]
C0027051
UMLS CUI [3]
C0038454
acute infections, tumor, severe arrhythmia, mental disease, drug or alcohol abuse
Descripción

Communicable Disease | Malignant Neoplasms | Cardiac Arrhythmia Severe | Mental disorders | Substance Use Disorders

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0006826
UMLS CUI [3,1]
C0003811
UMLS CUI [3,2]
C0205082
UMLS CUI [4]
C0004936
UMLS CUI [5]
C0038586
history of hepatitis or cirrhosis
Descripción

Hepatitis | Liver Cirrhosis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0019158
UMLS CUI [2]
C0023890
history of severe kidney disease
Descripción

Kidney Disease Severe

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0022658
UMLS CUI [1,2]
C0205082
pregnant, lactation
Descripción

Pregnancy | Breast Feeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
enrolled in other trials in 3 months
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568
any obstacles of follow-up or compliance
Descripción

Follow-up Limited | Compliance behavior Limited

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C0439801
UMLS CUI [2,1]
C1321605
UMLS CUI [2,2]
C0439801
Volver a la parte superior de la página

Similar models

Eligibility Hypertension NCT00847262

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
information consent signed
boolean
C0021430 (UMLS CUI [1])
Age
Item
aged 30~70 years
boolean
C0001779 (UMLS CUI [1])
Antihypertensive therapy Absent | Antihypertensive therapy | Systolic Pressure | Diastolic blood pressure
Item
for whom without anti-hypertensive therapy in 2 weeks：140mmhg≤sbp＜180mmhg，或90mmhg≤dbp＜110mmhg. for whom with anti-hypertensive therapies in 2 weeks：sbp＜180mmhg, 且dbp＜110mmhg
boolean
C0585941 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0585941 (UMLS CUI [2])
C0871470 (UMLS CUI [3])
C0428883 (UMLS CUI [4])
Waist Circumference | Gender
Item
waist circumference higher than 90cm in men, 80cm in women
boolean
C0455829 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
Diabetes Mellitus
Item
diagnosed diabetes
boolean
C0011849 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Hypertensive disease CTCAE Grades | Systolic Pressure | Diastolic blood pressure
Item
grade 3 hypertension: sbp≥180mmhg, or dbp≥110mmhg
boolean
C0020538 (UMLS CUI [1,1])
C1516728 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Waist Circumference | Gender
Item
waist circumference less than 90cm in men, 80cm in women
boolean
C0455829 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
Hypersensitivity Investigational New Drugs
Item
known allergy or hypersensitivity to trial drugs
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
Heart failure New York Heart Association Classification | Myocardial Infarction | Cerebrovascular accident
Item
nyha grade ⅱ~ⅳ heart failure, myocardial infarction or cerebrovascular accident in 1 year preceding the trial
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C0027051 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
Communicable Disease | Malignant Neoplasms | Cardiac Arrhythmia Severe | Mental disorders | Substance Use Disorders
Item
acute infections, tumor, severe arrhythmia, mental disease, drug or alcohol abuse
boolean
C0009450 (UMLS CUI [1])
C0006826 (UMLS CUI [2])
C0003811 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0004936 (UMLS CUI [4])
C0038586 (UMLS CUI [5])
Hepatitis | Liver Cirrhosis
Item
history of hepatitis or cirrhosis
boolean
C0019158 (UMLS CUI [1])
C0023890 (UMLS CUI [2])
Kidney Disease Severe
Item
history of severe kidney disease
boolean
C0022658 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant, lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Study Subject Participation Status
Item
enrolled in other trials in 3 months
boolean
C2348568 (UMLS CUI [1])
Follow-up Limited | Compliance behavior Limited
Item
any obstacles of follow-up or compliance
boolean
C3274571 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C1321605 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
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