ID

39388

Beschreibung

Model 4296 Left Ventricular (LV) Lead Study; ODM derived from: https://clinicaltrials.gov/show/NCT00927251

Link

https://clinicaltrials.gov/show/NCT00927251

Stichworte

Versionen (1)
  1. 06.01.20 06.01.20 -
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See clinicaltrials.gov

Hochgeladen am

6. Januar 2020

DOI

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Eligibility Heart Failure NCT00927251

Englisch

Eligibility Heart Failure NCT00927251

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
cardiac resynchronization therapy (crt)/cardiac resynchronization therapy-defibrillator (crt-d) indications according to the european society of cardiology/american college of cardiology/american heart association (esc/acc/aha) guidelines
Beschreibung

Indication Cardiac Resynchronization Therapy | Indication Implantation of CRT-D

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C1167956
UMLS CUI [2,1]
C3146298
UMLS CUI [2,2]
C1135480
on optimal medical treatment according to investigator opinion
Beschreibung

Therapy Optimal

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C2698651
indicated for implantable cardioverter defibrillator (icd) if crt-d is implanted
Beschreibung

Indication Implantable defibrillator | Implantation of CRT-D

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C0162589
UMLS CUI [2]
C1135480
patient consent
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
geographically stable
Beschreibung

Stable status Geographic

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0205360
UMLS CUI [1,2]
C1517526
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
left ventricular (lv) lead implant attempt in last 30 days
Beschreibung

Implant Attempt Ventricular Lead Left

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021102
UMLS CUI [1,2]
C1516084
UMLS CUI [1,3]
C2825199
UMLS CUI [1,4]
C0443246
unstable angina or acute myocardial infarction (mi) in past 30 days
Beschreibung

Angina, Unstable | Myocardial Infarction

Datentyp

boolean

Alias
UMLS CUI [1]
C0002965
UMLS CUI [2]
C0027051
coronary artery bypass graft (cabg) or percutaneous transluminal coronary angioplasty (ptca) in past 90 days
Beschreibung

Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention

Datentyp

boolean

Alias
UMLS CUI [1]
C0010055
UMLS CUI [2]
C1532338
contraindicated for transvenous pacing
Beschreibung

Medical contraindication Cardiac transvenous pacemaker

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0336574
heart transplant
Beschreibung

Heart Transplantation

Datentyp

boolean

Alias
UMLS CUI [1]
C0018823
contraindicated for less than 1 milligram (mg) dexamethasone acetate
Beschreibung

Medical contraindication Dexamethasone acetate Dose

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0057598
UMLS CUI [1,3]
C0178602
enrolled or intends to participate in concurrent drug and/or device study which would confound results
Beschreibung

Study Subject Participation Status | Investigational New Drug Interferes with Research results | Investigational Medical Device Interferes with Research results

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0013230
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0683954
UMLS CUI [3,1]
C2346570
UMLS CUI [3,2]
C0521102
UMLS CUI [3,3]
C0683954
life expectancy shorter than duration of the study
Beschreibung

Life Expectancy Less Than Planned Trial Duration

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0023671
UMLS CUI [1,2]
C0439092
UMLS CUI [1,3]
C4288390
exclusion criteria required by local law
Beschreibung

Exclusion Criteria Law Local

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C0220866
UMLS CUI [1,3]
C0205276
unable to tolerate urgent thoracotomy
Beschreibung

Thoracotomy Receive Unable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0039991
UMLS CUI [1,2]
C1514756
UMLS CUI [1,3]
C1299582
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Ähnliche Modelle

Eligibility Heart Failure NCT00927251

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Indication Cardiac Resynchronization Therapy | Indication Implantation of CRT-D
Item
cardiac resynchronization therapy (crt)/cardiac resynchronization therapy-defibrillator (crt-d) indications according to the european society of cardiology/american college of cardiology/american heart association (esc/acc/aha) guidelines
boolean
C3146298 (UMLS CUI [1,1])
C1167956 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C1135480 (UMLS CUI [2,2])
Therapy Optimal
Item
on optimal medical treatment according to investigator opinion
boolean
C0087111 (UMLS CUI [1,1])
C2698651 (UMLS CUI [1,2])
Indication Implantable defibrillator | Implantation of CRT-D
Item
indicated for implantable cardioverter defibrillator (icd) if crt-d is implanted
boolean
C3146298 (UMLS CUI [1,1])
C0162589 (UMLS CUI [1,2])
C1135480 (UMLS CUI [2])
Informed Consent
Item
patient consent
boolean
C0021430 (UMLS CUI [1])
Stable status Geographic
Item
geographically stable
boolean
C0205360 (UMLS CUI [1,1])
C1517526 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Implant Attempt Ventricular Lead Left
Item
left ventricular (lv) lead implant attempt in last 30 days
boolean
C0021102 (UMLS CUI [1,1])
C1516084 (UMLS CUI [1,2])
C2825199 (UMLS CUI [1,3])
C0443246 (UMLS CUI [1,4])
Angina, Unstable | Myocardial Infarction
Item
unstable angina or acute myocardial infarction (mi) in past 30 days
boolean
C0002965 (UMLS CUI [1])
C0027051 (UMLS CUI [2])
Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention
Item
coronary artery bypass graft (cabg) or percutaneous transluminal coronary angioplasty (ptca) in past 90 days
boolean
C0010055 (UMLS CUI [1])
C1532338 (UMLS CUI [2])
Medical contraindication Cardiac transvenous pacemaker
Item
contraindicated for transvenous pacing
boolean
C1301624 (UMLS CUI [1,1])
C0336574 (UMLS CUI [1,2])
Heart Transplantation
Item
heart transplant
boolean
C0018823 (UMLS CUI [1])
Medical contraindication Dexamethasone acetate Dose
Item
contraindicated for less than 1 milligram (mg) dexamethasone acetate
boolean
C1301624 (UMLS CUI [1,1])
C0057598 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
Study Subject Participation Status | Investigational New Drug Interferes with Research results | Investigational Medical Device Interferes with Research results
Item
enrolled or intends to participate in concurrent drug and/or device study which would confound results
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0683954 (UMLS CUI [2,3])
C2346570 (UMLS CUI [3,1])
C0521102 (UMLS CUI [3,2])
C0683954 (UMLS CUI [3,3])
Life Expectancy Less Than Planned Trial Duration
Item
life expectancy shorter than duration of the study
boolean
C0023671 (UMLS CUI [1,1])
C0439092 (UMLS CUI [1,2])
C4288390 (UMLS CUI [1,3])
Exclusion Criteria Law Local
Item
exclusion criteria required by local law
boolean
C0680251 (UMLS CUI [1,1])
C0220866 (UMLS CUI [1,2])
C0205276 (UMLS CUI [1,3])
Thoracotomy Receive Unable
Item
unable to tolerate urgent thoracotomy
boolean
C0039991 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
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