ID

42791

Descrição

Measuring G Protein-coupled Receptor Kinase-2 (GRK2) in the Blood to Diagnose and Treat Patients With Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT00419965

Link

https://clinicaltrials.gov/show/NCT00419965

Palavras-chave

  1. 22/03/2017 22/03/2017 -
  2. 17/09/2021 17/09/2021 -
Transferido a

17 de setembro de 2021

DOI

Para um pedido faça login.

Licença

Creative Commons BY 4.0

Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Eligibility Heart Failure NCT00419965

Eligibility Heart Failure NCT00419965

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
normal controls: individuals without hf, hypertension, diabetes, hyperlipidemia, coronary artery disease or obesity;
Descrição

Heart failure Absent | Hypertensive disease Absent | Diabetes Mellitus Absent | Hyperlipidemia Absent | Coronary Artery Disease Absent | Obesity Absent

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0020538
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C0011849
UMLS CUI [3,2]
C0332197
UMLS CUI [4,1]
C0020473
UMLS CUI [4,2]
C0332197
UMLS CUI [5,1]
C1956346
UMLS CUI [5,2]
C0332197
UMLS CUI [6,1]
C0028754
UMLS CUI [6,2]
C0332197
group i: symptomatic subjects with reduced lv function, hf symptoms, ef ≤ 40%.
Descrição

Study Subject Symptomatic | Impaired left ventricular function | Heart failure Symptoms | Ejection fraction

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0681850
UMLS CUI [1,2]
C0231220
UMLS CUI [2]
C0242698
UMLS CUI [3,1]
C0018801
UMLS CUI [3,2]
C1457887
UMLS CUI [4]
C2700378
group ii: asymptomatic patients with lv dysfunction, no hf symptoms (nyha class i and ats score 0 or 1, ef ≤ 40%.
Descrição

Patients Asymptomatic | Ventricular Dysfunction, Left | Heart failure New York Heart Association Classification | Ejection fraction

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0231221
UMLS CUI [2]
C0242698
UMLS CUI [3,1]
C0018801
UMLS CUI [3,2]
C1275491
UMLS CUI [4]
C2700378
group iii: symptomatic subjects with preserved lv function, hf symptoms, ef ≥ 50%, and diastolic dysfunction.
Descrição

Study Subject Symptomatic | Left Ventricular Function Normal | Heart failure Symptoms | Ejection fraction | Diastolic dysfunction

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0681850
UMLS CUI [1,2]
C0231220
UMLS CUI [2,1]
C0080310
UMLS CUI [2,2]
C0205307
UMLS CUI [3,1]
C0018801
UMLS CUI [3,2]
C1457887
UMLS CUI [4]
C2700378
UMLS CUI [5]
C0520863
group iv: asymptomatic high risk subjects - individuals with normal heart function, no hf symptoms (nyha class i and ats score 0 or 1), preserved lv function (ef ≥ 50%), no diastolic dysfunction. also possess one or more cardiovascular high risk factors: diagnosis of diabetes; hyperlipidemia; coronary artery disease; renal insufficiency; hypertension; age >70 years
Descrição

Study Subject Asymptomatic High risk | Cardiac function | Heart failure New York Heart Association Classification | Left Ventricular Function Normal | Ejection fraction | Diastolic dysfunction Absent | High risk factors Cardiovascular Quantity | Diabetes Mellitus | Hyperlipidemia | Coronary Artery Disease | Renal Insufficiency | Hypertensive disease | Age

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0681850
UMLS CUI [1,2]
C0231221
UMLS CUI [1,3]
C0332167
UMLS CUI [2]
C0232164
UMLS CUI [3,1]
C0018801
UMLS CUI [3,2]
C1275491
UMLS CUI [4,1]
C0080310
UMLS CUI [4,2]
C0205307
UMLS CUI [5]
C2700378
UMLS CUI [6,1]
C0520863
UMLS CUI [6,2]
C0332197
UMLS CUI [7,1]
C1830377
UMLS CUI [7,2]
C3887460
UMLS CUI [7,3]
C1265611
UMLS CUI [8]
C0011849
UMLS CUI [9]
C0020473
UMLS CUI [10]
C1956346
UMLS CUI [11]
C1565489
UMLS CUI [12]
C0020538
UMLS CUI [13]
C0001779
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy
Descrição

Pregnancy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032961
not providing consent
Descrição

Informed Consent Missing

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1705492
inability to provide consent
Descrição

Informed Consent Unable

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
participation in a clinical study involving an experimental therapy.
Descrição

Study Subject Participation Status | Therapy, Investigational

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0949266

Similar models

Eligibility Heart Failure NCT00419965

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Heart failure Absent | Hypertensive disease Absent | Diabetes Mellitus Absent | Hyperlipidemia Absent | Coronary Artery Disease Absent | Obesity Absent
Item
normal controls: individuals without hf, hypertension, diabetes, hyperlipidemia, coronary artery disease or obesity;
boolean
C0018801 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0020538 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0011849 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
C0020473 (UMLS CUI [4,1])
C0332197 (UMLS CUI [4,2])
C1956346 (UMLS CUI [5,1])
C0332197 (UMLS CUI [5,2])
C0028754 (UMLS CUI [6,1])
C0332197 (UMLS CUI [6,2])
Study Subject Symptomatic | Impaired left ventricular function | Heart failure Symptoms | Ejection fraction
Item
group i: symptomatic subjects with reduced lv function, hf symptoms, ef ≤ 40%.
boolean
C0681850 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0242698 (UMLS CUI [2])
C0018801 (UMLS CUI [3,1])
C1457887 (UMLS CUI [3,2])
C2700378 (UMLS CUI [4])
Patients Asymptomatic | Ventricular Dysfunction, Left | Heart failure New York Heart Association Classification | Ejection fraction
Item
group ii: asymptomatic patients with lv dysfunction, no hf symptoms (nyha class i and ats score 0 or 1, ef ≤ 40%.
boolean
C0030705 (UMLS CUI [1,1])
C0231221 (UMLS CUI [1,2])
C0242698 (UMLS CUI [2])
C0018801 (UMLS CUI [3,1])
C1275491 (UMLS CUI [3,2])
C2700378 (UMLS CUI [4])
Study Subject Symptomatic | Left Ventricular Function Normal | Heart failure Symptoms | Ejection fraction | Diastolic dysfunction
Item
group iii: symptomatic subjects with preserved lv function, hf symptoms, ef ≥ 50%, and diastolic dysfunction.
boolean
C0681850 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0080310 (UMLS CUI [2,1])
C0205307 (UMLS CUI [2,2])
C0018801 (UMLS CUI [3,1])
C1457887 (UMLS CUI [3,2])
C2700378 (UMLS CUI [4])
C0520863 (UMLS CUI [5])
Study Subject Asymptomatic High risk | Cardiac function | Heart failure New York Heart Association Classification | Left Ventricular Function Normal | Ejection fraction | Diastolic dysfunction Absent | High risk factors Cardiovascular Quantity | Diabetes Mellitus | Hyperlipidemia | Coronary Artery Disease | Renal Insufficiency | Hypertensive disease | Age
Item
group iv: asymptomatic high risk subjects - individuals with normal heart function, no hf symptoms (nyha class i and ats score 0 or 1), preserved lv function (ef ≥ 50%), no diastolic dysfunction. also possess one or more cardiovascular high risk factors: diagnosis of diabetes; hyperlipidemia; coronary artery disease; renal insufficiency; hypertension; age >70 years
boolean
C0681850 (UMLS CUI [1,1])
C0231221 (UMLS CUI [1,2])
C0332167 (UMLS CUI [1,3])
C0232164 (UMLS CUI [2])
C0018801 (UMLS CUI [3,1])
C1275491 (UMLS CUI [3,2])
C0080310 (UMLS CUI [4,1])
C0205307 (UMLS CUI [4,2])
C2700378 (UMLS CUI [5])
C0520863 (UMLS CUI [6,1])
C0332197 (UMLS CUI [6,2])
C1830377 (UMLS CUI [7,1])
C3887460 (UMLS CUI [7,2])
C1265611 (UMLS CUI [7,3])
C0011849 (UMLS CUI [8])
C0020473 (UMLS CUI [9])
C1956346 (UMLS CUI [10])
C1565489 (UMLS CUI [11])
C0020538 (UMLS CUI [12])
C0001779 (UMLS CUI [13])
Item Group
C0680251 (UMLS CUI)
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Informed Consent Missing
Item
not providing consent
boolean
C0021430 (UMLS CUI [1,1])
C1705492 (UMLS CUI [1,2])
Informed Consent Unable
Item
inability to provide consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Study Subject Participation Status | Therapy, Investigational
Item
participation in a clinical study involving an experimental therapy.
boolean
C2348568 (UMLS CUI [1])
C0949266 (UMLS CUI [2])

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

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