ID

33164

Descripción

Regulation of Tissue Lipolysis by Insulin in Type 2 Diabetes; ODM derived from: https://clinicaltrials.gov/show/NCT01680133

Link

https://clinicaltrials.gov/show/NCT01680133

Palabras clave

  1. 30/11/18 30/11/18 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

30 de noviembre de 2018

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Type 2 Diabetes NCT01680133

Eligibility Type 2 Diabetes NCT01680133

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
caucasian
Descripción

Caucasian

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0043157
normal blood pressure (sbp 100-140 mmhg, dbp 60-90 mmhg)
Descripción

Normal blood pressure | Systolic Pressure | Diastolic blood pressure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2712122
UMLS CUI [2]
C0871470
UMLS CUI [3]
C0428883
weight stable in last 3 months
Descripción

Stable body weight

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0517386
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
smokers
Descripción

Tobacco use

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0543414
people with intensive fitness training (e.g. athletes > 3 times/week)
Descripción

Physical fitness training With intensity

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1535955
UMLS CUI [1,2]
C0522510
history of cardiovascular diseases
Descripción

Cardiovascular Diseases

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007222
bleeding disorders
Descripción

Blood Coagulation Disorders

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005779
use of medication interfering with the study endpoints/hypotheses (e.g. beta-blockers)
Descripción

Pharmaceutical Preparations Interfere with End Point | Pharmaceutical Preparations Interfere with Clinical Trial Hypothesis | Adrenergic beta-1 Receptor Antagonists

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C2349179
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0008976
UMLS CUI [2,4]
C1512571
UMLS CUI [3]
C0304516
not to be able to understand the study information
Descripción

Study Protocol Comprehension Unable

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0162340
UMLS CUI [1,3]
C1299582
subjects on a special diet or vegetarian
Descripción

On special diet | Vegetarian

Tipo de datos

boolean

Alias
UMLS CUI [1]
C3164710
UMLS CUI [2]
C0042441
blood donation 2 months prior to the study and during the study
Descripción

Blood Donation

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005794
participating in an other study
Descripción

Study Subject Participation Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Type 2 Diabetes NCT01680133

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Caucasian
Item
caucasian
boolean
C0043157 (UMLS CUI [1])
Normal blood pressure | Systolic Pressure | Diastolic blood pressure
Item
normal blood pressure (sbp 100-140 mmhg, dbp 60-90 mmhg)
boolean
C2712122 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Stable body weight
Item
weight stable in last 3 months
boolean
C0517386 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Tobacco use
Item
smokers
boolean
C0543414 (UMLS CUI [1])
Physical fitness training With intensity
Item
people with intensive fitness training (e.g. athletes > 3 times/week)
boolean
C1535955 (UMLS CUI [1,1])
C0522510 (UMLS CUI [1,2])
Cardiovascular Diseases
Item
history of cardiovascular diseases
boolean
C0007222 (UMLS CUI [1])
Blood Coagulation Disorders
Item
bleeding disorders
boolean
C0005779 (UMLS CUI [1])
Pharmaceutical Preparations Interfere with End Point | Pharmaceutical Preparations Interfere with Clinical Trial Hypothesis | Adrenergic beta-1 Receptor Antagonists
Item
use of medication interfering with the study endpoints/hypotheses (e.g. beta-blockers)
boolean
C0013227 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C2349179 (UMLS CUI [1,3])
C0013227 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
C1512571 (UMLS CUI [2,4])
C0304516 (UMLS CUI [3])
Study Protocol Comprehension Unable
Item
not to be able to understand the study information
boolean
C2348563 (UMLS CUI [1,1])
C0162340 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
On special diet | Vegetarian
Item
subjects on a special diet or vegetarian
boolean
C3164710 (UMLS CUI [1])
C0042441 (UMLS CUI [2])
Blood Donation
Item
blood donation 2 months prior to the study and during the study
boolean
C0005794 (UMLS CUI [1])
Study Subject Participation Status
Item
participating in an other study
boolean
C2348568 (UMLS CUI [1])

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