ID

44675

Beschreibung

Use of the Self-Expanding CoreValve Prosthesis without Predilation in Patients with Significantly IMPaired Left-VentrIcular Ejection Fraction for Transcatheter Aortic Valve Implantation Study. Form is used in following visits: - Baseline Projektleiter (LKP): Prof. Dr. med. Georg Nickenig Medizinische Klinik und Poliklinik II Sigmund-Freud-Str. 25, 53125 Bonn Tel. 0228-287-15217, Fax 0228-287-16423 Email: georg.nickenig@ukb.uni-bonn.de

Stichworte

Versionen (2)
  1. 01.02.16 01.02.16 -
  2. 27.09.21 27.09.21 -
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27. September 2021

DOI

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Eligiblity Criteria SIMPLIFy TAVI Transcatheter Aortic Valve Implantation Without Predilation NCT01539746

Englisch

Eligiblity Criteria NCT01539746

1 Formulare  
Date of visit
Beschreibung

Date of visit

Alias
UMLS CUI-1
C1320303
Date of visit
Beschreibung

Date of visit

Datentyp

date

Alias
UMLS CUI [1]
C1320303
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
LVEF ≤35%
Beschreibung

LVEF ≤35%

Datentyp

boolean

Alias
UMLS CUI [1]
C0428772
Aortic valve stenosis with an aortic valve area <1 cm2 (<0,6 cm3/m2)
Beschreibung

Aortic valve stenosis with an aortic valve area <1 cm2 (<0,6 cm3/m2)

Datentyp

boolean

Alias
UMLS CUI [1]
C0003507
Males or females at least 18 years of age
Beschreibung

Males or females at least 18 years of age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
Logistic EuroSCORE ≥15% and age ≥75 years or if age <75 years: logistic EuroSCORE ≥20% and/or a significant contraindication for open heart surgery (e.g., porcelain aorta or severe COPD)
Beschreibung

Logistic EuroSCORE ≥15% and age ≥75 years or if age <75 years: logistic EuroSCORE ≥20% and/or a significant contraindication for open heart surgery (e.g., porcelain aorta or severe COPD)

Datentyp

boolean

Alias
UMLS CUI [1]
C3164744
Signed informed consent
Beschreibung

Signed informed consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Patients with a device regulating the heart rhythm by pacing (e.g. pacemaker, resynchronization device, implanted defibrillator) with atrioventricular block >= 1. degree and ventricular pacing rate > 10%
Beschreibung

Patients with a device regulating the heart rhythm by pacing (e.g. pacemaker, resynchronization device, implanted defibrillator) with atrioventricular block >= 1. degree and ventricular pacing rate > 10%

Datentyp

boolean

Alias
UMLS CUI [1]
C0162589
UMLS CUI [2]
C0004245
UMLS CUI [3]
C2016308
Patients with implanted pacemaker because of AV block >= Degree II or Cardiac Resynchronization Therapy (CRT)
Beschreibung

Patients with implanted pacemaker because of AV block >= Degree II or Cardiac Resynchronization Therapy (CRT)

Datentyp

boolean

Alias
UMLS CUI [1]
C0030163
UMLS CUI [2]
C0004245
UMLS CUI [3]
C1167956
Lack of written informed consent, severe mental disorder, drug/alcohol addiction
Beschreibung

Lack of written informed consent, severe mental disorder, drug/alcohol addiction

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C1321605
UMLS CUI [2,2]
C0439801
UMLS CUI [2,3]
C0009488
UMLS CUI [3]
C0038586
Life expectancy < 1 year
Beschreibung

Life expectancy < 1 year

Datentyp

boolean

Alias
UMLS CUI [1]
C0023671
Hypersensitivity or contraindication to acetyl salicyl acid, heparin, ticlopidine, clopidogrel, nitinol or sensitivity to contrast media that cannot be adequately premedicated
Beschreibung

Hypersensitivity or contraindication to acetyl salicyl acid, heparin, ticlopidine, clopidogrel, nitinol or sensitivity to contrast media that cannot be adequately premedicated

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0004057
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0019134
UMLS CUI [3,1]
C0020517
UMLS CUI [3,2]
C0040207
UMLS CUI [4,1]
C0020517
UMLS CUI [4,2]
C0070166
UMLS CUI [5,1]
C0020517
UMLS CUI [5,2]
C0068790
UMLS CUI [6,1]
C0020517
UMLS CUI [6,2]
C0009924
Recent myocardial infarction (STEMI within the last 3 months)
Beschreibung

Recent myocardial infarction (STEMI within the last 3 months)

Datentyp

boolean

Alias
UMLS CUI [1]
C0027051
Left ventricular or atrial thrombus
Beschreibung

Left ventricular or atrial thrombus

Datentyp

boolean

Alias
UMLS CUI [1]
C0587044
UMLS CUI [2]
C0340517
Uncontrolled atrial fibrillation (heart rate > 140/Min)
Beschreibung

Uncontrolled atrial fibrillation (heart rate > 140/Min)

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0009450
Mitral or tricuspidal valvular insufficiency (> grade II)
Beschreibung

Mitral or tricuspidal valvular insufficiency (> grade II)

Datentyp

boolean

Alias
UMLS CUI [1]
C0026266
UMLS CUI [2]
C0040961
Previous aortic valve replacement with mechanical valve
Beschreibung

Previous aortic valve replacement with mechanical valve

Datentyp

boolean

Alias
UMLS CUI [1]
C0003506
Evolutive or recent cerebrovascular event (within the last 3 months)
Beschreibung

Evolutive or recent cerebrovascular event (within the last 3 months)

Datentyp

boolean

Alias
UMLS CUI [1]
C0038454
Vascular conditions that make insertion and endovascular access to the aortic valve impossible
Beschreibung

Vascular conditions that make insertion and endovascular access to the aortic valve impossible

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C2712690
Symptomatic carotid or vertebral arterial narrowing (>70%) disease
Beschreibung

Symptomatic carotid or vertebral arterial narrowing (>70%) disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0007282
UMLS CUI [2]
C0042568
Abdominal or thoracic aortic aneurysm in the path of the delivery system
Beschreibung

Abdominal or thoracic aortic aneurysm in the path of the delivery system

Datentyp

boolean

Alias
UMLS CUI [1]
C0162871
UMLS CUI [2]
C0162872
Bleeding diathesis or contraindication to blood transfusion
Beschreibung

Bleeding diathesis or contraindication to blood transfusion

Datentyp

boolean

Alias
UMLS CUI [1]
C0005779
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0005841
Active gastritis or peptic ulcer disease
Beschreibung

Active gastritis or peptic ulcer disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0017152
UMLS CUI [2]
C0030920
Severely impaired renal function, GFR < 30 ml/min
Beschreibung

Severely impaired renal function, GFR < 30 ml/min

Datentyp

boolean

Alias
UMLS CUI [1]
C1316377
Sepsis including acute endocarditis
Beschreibung

sepsis or acute endocarditis

Datentyp

boolean

Alias
UMLS CUI [1]
C0243026
UMLS CUI [2]
C0375268
Partition in another clinical trial
Beschreibung

Partition in another clinical trial

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
High probability of non-compliant study participation
Beschreibung

High probability of non-compliant study participation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
Pregnancy
Beschreibung

Pregnancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
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Ähnliche Modelle

Eligiblity Criteria NCT01539746

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Date of visit
C1320303 (UMLS CUI-1)
date of visit
Item
Date of visit
date
C1320303 (UMLS CUI [1])
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
LVEF
Item
LVEF ≤35%
boolean
C0428772 (UMLS CUI [1])
aortic valve stenosis
Item
Aortic valve stenosis with an aortic valve area <1 cm2 (<0,6 cm3/m2)
boolean
C0003507 (UMLS CUI [1])
age
Item
Males or females at least 18 years of age
boolean
C0001779 (UMLS CUI [1])
logistic euroSCORE
Item
Logistic EuroSCORE ≥15% and age ≥75 years or if age <75 years: logistic EuroSCORE ≥20% and/or a significant contraindication for open heart surgery (e.g., porcelain aorta or severe COPD)
boolean
C3164744 (UMLS CUI [1])
signed informed consent
Item
Signed informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
ICD
Item
Patients with a device regulating the heart rhythm by pacing (e.g. pacemaker, resynchronization device, implanted defibrillator) with atrioventricular block >= 1. degree and ventricular pacing rate > 10%
boolean
C0162589 (UMLS CUI [1])
C0004245 (UMLS CUI [2])
C2016308 (UMLS CUI [3])
implanted pacemaker or CRT
Item
Patients with implanted pacemaker because of AV block >= Degree II or Cardiac Resynchronization Therapy (CRT)
boolean
C0030163 (UMLS CUI [1])
C0004245 (UMLS CUI [2])
C1167956 (UMLS CUI [3])
mental disorder or drug addiction
Item
Lack of written informed consent, severe mental disorder, drug/alcohol addiction
boolean
C0021430 (UMLS CUI [1])
C1321605 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0009488 (UMLS CUI [2,3])
C0038586 (UMLS CUI [3])
life expectancy
Item
Life expectancy < 1 year
boolean
C0023671 (UMLS CUI [1])
hypersensibility or contraindication
Item
Hypersensitivity or contraindication to acetyl salicyl acid, heparin, ticlopidine, clopidogrel, nitinol or sensitivity to contrast media that cannot be adequately premedicated
boolean
C0020517 (UMLS CUI [1,1])
C0004057 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0019134 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C0040207 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C0070166 (UMLS CUI [4,2])
C0020517 (UMLS CUI [5,1])
C0068790 (UMLS CUI [5,2])
C0020517 (UMLS CUI [6,1])
C0009924 (UMLS CUI [6,2])
myocardial infarction
Item
Recent myocardial infarction (STEMI within the last 3 months)
boolean
C0027051 (UMLS CUI [1])
left ventricular or atrial thrombus
Item
Left ventricular or atrial thrombus
boolean
C0587044 (UMLS CUI [1])
C0340517 (UMLS CUI [2])
uncontrolled atrial fibrillation
Item
Uncontrolled atrial fibrillation (heart rate > 140/Min)
boolean
C0004238 (UMLS CUI [1,1])
C0009450 (UMLS CUI [1,2])
mitral or tricuspidal valvular insufficiency
Item
Mitral or tricuspidal valvular insufficiency (> grade II)
boolean
C0026266 (UMLS CUI [1])
C0040961 (UMLS CUI [2])
aortic valve replacement
Item
Previous aortic valve replacement with mechanical valve
boolean
C0003506 (UMLS CUI [1])
cerebrovascular event
Item
Evolutive or recent cerebrovascular event (within the last 3 months)
boolean
C0038454 (UMLS CUI [1])
inadequate catheter
Item
Vascular conditions that make insertion and endovascular access to the aortic valve impossible
boolean
C0021430 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C2712690 (UMLS CUI [1,3])
symptomatic carotid
Item
Symptomatic carotid or vertebral arterial narrowing (>70%) disease
boolean
C0007282 (UMLS CUI [1])
C0042568 (UMLS CUI [2])
abdominal or thoracic aortic aneurysm
Item
Abdominal or thoracic aortic aneurysm in the path of the delivery system
boolean
C0162871 (UMLS CUI [1])
C0162872 (UMLS CUI [2])
bleeding diathesis
Item
Bleeding diathesis or contraindication to blood transfusion
boolean
C0005779 (UMLS CUI [1])
C1301624 (UMLS CUI [2,1])
C0005841 (UMLS CUI [2,2])
active gastritis or peptic ulcer disease
Item
Active gastritis or peptic ulcer disease
boolean
C0017152 (UMLS CUI [1])
C0030920 (UMLS CUI [2])
renal function
Item
Severely impaired renal function, GFR < 30 ml/min
boolean
C1316377 (UMLS CUI [1])
sepsis or acute endocarditis
Item
Sepsis including acute endocarditis
boolean
C0243026 (UMLS CUI [1])
C0375268 (UMLS CUI [2])
partition in another trial
Item
Partition in another clinical trial
boolean
C2348568 (UMLS CUI [1])
limited compliance expectable
Item
High probability of non-compliant study participation
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
pregnancy
Item
Pregnancy
boolean
C0032961 (UMLS CUI [1])
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