Informatie:
Fout:
ID
20980
Beschrijving
MINERVA: MINimizE Right Ventricular Pacing to Prevent Atrial Fibrillation and Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT00262119
Link
https://clinicaltrials.gov/show/NCT00262119
Trefwoorden
Versies (1)
- 02-04-17 02-04-17 -
Geüploaded op
2 april 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT00262119
Eligibility Atrial Fibrillation NCT00262119
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT00262119
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
dual chamber pacing indications
Item
class i/class ii indications for dual chamber pacing
boolean
C0494014 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
C0392360 (UMLS CUI [1,2])
previous implant of enrhythm dual chamber implantable pulse generator
Item
previous implant of an enrhythm dual chamber implantable pulse generator (ipg) since maximum 2 weeks
boolean
C0493526 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C1442457 (UMLS CUI [1,3])
C0205156 (UMLS CUI [1,2])
C1442457 (UMLS CUI [1,3])
history of atrial arrhythmias
Item
history of atrial arrhythmias (at least one electrocardiogram [ecg] or holter documented episodes in the last 12 months)
boolean
C0262926 (UMLS CUI [1,1])
C0013798 (UMLS CUI [1,2])
C0085611 (UMLS CUI [1,3])
C0013798 (UMLS CUI [1,2])
C0085611 (UMLS CUI [1,3])
age under 18
Item
less than 18 years of age
boolean
C0001779 (UMLS CUI [1])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
informed consent ability
Item
unwilling or unable to give informed consent or to commit to follow-up schedule
boolean
C0021430 (UMLS CUI [1,1])
C0085732 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,2])
study participation limited
Item
medical conditions that preclude protocol required testing or limit study participation
boolean
C0008972 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
C0679823 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
other clinical study
Item
enrolled or intend to participate in another clinical trial during the course of this study
boolean
C2348568 (UMLS CUI [1])
life expectancy
Item
a life expectancy of less than 2 years
boolean
C0023671 (UMLS CUI [1])
implantable cardioverter defibrillator or cardiac resynchronization therapy possible
Item
patient is a candidate for an implantable cardioverter defibrillator (icd) or cardiac resynchronization therapy (crt) device implant
boolean
C0162589 (UMLS CUI [1,1])
C0332149 (UMLS CUI [1,2])
C1167956 (UMLS CUI [2,1])
C0332149 (UMLS CUI [2,2])
C0332149 (UMLS CUI [1,2])
C1167956 (UMLS CUI [2,1])
C0332149 (UMLS CUI [2,2])
major cardiac surgery anticipated
Item
anticipated major cardiac surgery within the course of this study
boolean
C0018821 (UMLS CUI [1,1])
C3840775 (UMLS CUI [1,2])
C3840775 (UMLS CUI [1,2])
degree 3 av-block or previous av node ablation
Item
permanent iii degree av-block or history of av node ablation
boolean
C0151517 (UMLS CUI [1])
C0262926 (UMLS CUI [2,1])
C3275044 (UMLS CUI [2,2])
C0262926 (UMLS CUI [2,1])
C3275044 (UMLS CUI [2,2])
permanent artrial fibrillation
Item
history of permanent af (as defined below)
boolean
C0004238 (UMLS CUI [1])
undefined item
Item
af ablation (left pulmonary veins) or other cardiac surgery < 3 months
boolean
C2702800 (UMLS CUI [1])
C0018821 (UMLS CUI [2])
C0018821 (UMLS CUI [2])
implant of defibrillator or pacemaker
Item
prior implant of defibrillator device or pacemaker (apart from enrhythm ipg implanted within two weeks)
boolean
C0162589 (UMLS CUI [1])
C0182148 (UMLS CUI [2])
C0182148 (UMLS CUI [2])
uncontrolled hyperthyroidism
Item
uncontrolled hyperthyroidism
boolean
C0020550 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0205318 (UMLS CUI [1,2])