ID

29580

Beschrijving

Torsion Optimization to Reduce Symptoms and Improve Outcomes in Non-responders; ODM derived from: https://clinicaltrials.gov/show/NCT00867984

Link

https://clinicaltrials.gov/show/NCT00867984

Trefwoorden

Versies (2)
  1. 07-04-18 07-04-18 -
  2. 07-04-18 07-04-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

7 april 2018

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Heart Failure, Congestive NCT00867984

Engels

Eligibility Heart Failure, Congestive NCT00867984

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
non-response to crt as indicated,
Beschrijving

Cardiac Resynchronization Therapy Unresponsive to Treatment

Datatype

boolean

Alias
UMLS CUI [1,1]
C1167956
UMLS CUI [1,2]
C0205269
stable doses of ace i / arb and beta-blocker for ≥ 2 months, &
Beschrijving

Angiotensin-Converting Enzyme Inhibitors Dose Stable | Angiotensin II receptor antagonist Dose Stable | Adrenergic beta-1 Receptor Antagonists Dose Stable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003015
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0205360
UMLS CUI [2,1]
C0521942
UMLS CUI [2,2]
C0178602
UMLS CUI [2,3]
C0205360
UMLS CUI [3,1]
C0304516
UMLS CUI [3,2]
C0178602
UMLS CUI [3,3]
C0205360
controlled heart rate if in atrial fibrillation.
Beschrijving

Heart rate Controlled | Atrial Fibrillation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018810
UMLS CUI [1,2]
C2587213
UMLS CUI [2]
C0004238
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
inadequate images to assess torsion
Beschrijving

Torsion Imaging Inadequate

Datatype

boolean

Alias
UMLS CUI [1,1]
C1956418
UMLS CUI [1,2]
C0011923
UMLS CUI [1,3]
C0205412
no significant augmentation in torsion with optimization
Beschrijving

Absence Torsion augmented

Datatype

boolean

Alias
UMLS CUI [1,1]
C0332197
UMLS CUI [1,2]
C1956418
UMLS CUI [1,3]
C0205217
unable or unwilling to provide informed consent,
Beschrijving

Informed Consent Unable | Informed Consent Unwilling

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0558080
medical condition other than hf likely to cause death within 6 months,
Beschrijving

Medical condition Causing Death | Exception Heart failure

Datatype

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0678227
UMLS CUI [1,3]
C0011065
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0018801
cardiac transplant planned,
Beschrijving

Heart Transplantation Planned

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018823
UMLS CUI [1,2]
C1301732
myocardial infarction or revascularization since crt implant.
Beschrijving

Myocardial Infarction Since Implantation of CRT-D | Myocardial Revascularization Since Implantation of CRT-D

Datatype

boolean

Alias
UMLS CUI [1,1]
C0027051
UMLS CUI [1,2]
C1711239
UMLS CUI [1,3]
C1135480
UMLS CUI [2,1]
C0027056
UMLS CUI [2,2]
C1711239
UMLS CUI [2,3]
C1135480
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Similar models

Eligibility Heart Failure, Congestive NCT00867984

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Cardiac Resynchronization Therapy Unresponsive to Treatment
Item
non-response to crt as indicated,
boolean
C1167956 (UMLS CUI [1,1])
C0205269 (UMLS CUI [1,2])
Angiotensin-Converting Enzyme Inhibitors Dose Stable | Angiotensin II receptor antagonist Dose Stable | Adrenergic beta-1 Receptor Antagonists Dose Stable
Item
stable doses of ace i / arb and beta-blocker for ≥ 2 months, &
boolean
C0003015 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0521942 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0205360 (UMLS CUI [2,3])
C0304516 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
C0205360 (UMLS CUI [3,3])
Heart rate Controlled | Atrial Fibrillation
Item
controlled heart rate if in atrial fibrillation.
boolean
C0018810 (UMLS CUI [1,1])
C2587213 (UMLS CUI [1,2])
C0004238 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Torsion Imaging Inadequate
Item
inadequate images to assess torsion
boolean
C1956418 (UMLS CUI [1,1])
C0011923 (UMLS CUI [1,2])
C0205412 (UMLS CUI [1,3])
Absence Torsion augmented
Item
no significant augmentation in torsion with optimization
boolean
C0332197 (UMLS CUI [1,1])
C1956418 (UMLS CUI [1,2])
C0205217 (UMLS CUI [1,3])
Informed Consent Unable | Informed Consent Unwilling
Item
unable or unwilling to provide informed consent,
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Medical condition Causing Death | Exception Heart failure
Item
medical condition other than hf likely to cause death within 6 months,
boolean
C3843040 (UMLS CUI [1,1])
C0678227 (UMLS CUI [1,2])
C0011065 (UMLS CUI [1,3])
C1705847 (UMLS CUI [2,1])
C0018801 (UMLS CUI [2,2])
Heart Transplantation Planned
Item
cardiac transplant planned,
boolean
C0018823 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Myocardial Infarction Since Implantation of CRT-D | Myocardial Revascularization Since Implantation of CRT-D
Item
myocardial infarction or revascularization since crt implant.
boolean
C0027051 (UMLS CUI [1,1])
C1711239 (UMLS CUI [1,2])
C1135480 (UMLS CUI [1,3])
C0027056 (UMLS CUI [2,1])
C1711239 (UMLS CUI [2,2])
C1135480 (UMLS CUI [2,3])
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