ID

42791

Beschreibung

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

Stichworte

Versionen (2)
  1. 22.03.17 22.03.17 -
  2. 17.09.21 17.09.21 -
Hochgeladen am

17. September 2021

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Heart Failure NCT00419965

Englisch

Eligibility Heart Failure NCT00419965

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

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

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

Datentyp

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%.
Beschreibung

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

Datentyp

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%.
Beschreibung

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

Datentyp

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.
Beschreibung

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

Datentyp

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
Beschreibung

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

Datentyp

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
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy
Beschreibung

Pregnancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
not providing consent
Beschreibung

Informed Consent Missing

Datentyp

boolean

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

Informed Consent Unable

Datentyp

boolean

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

Study Subject Participation Status | Therapy, Investigational

Datentyp

boolean

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

Eligibility Heart Failure NCT00419965

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])
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