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Fout:
ID
33292
Beschrijving
Management and Detection of Atrial Tachyarrhythmias in Patients Implanted With BIOTRONIK DX Systems; ODM derived from: https://clinicaltrials.gov/show/NCT01774357
Link
https://clinicaltrials.gov/show/NCT01774357
Trefwoorden
Versies (1)
- 04-12-18 04-12-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
4 december 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT01774357
Eligibility Atrial Fibrillation NCT01774357
- StudyEvent: Eligibility
Similar models
Eligibility Atrial Fibrillation NCT01774357
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Indication Implantation Single chamber cardioverter-defibrillator Primary Prevention | Indication Implantation Single chamber cardioverter-defibrillator Secondary Prevention
Item
indication for implantation of a single chamber icd (primary or secondary prevention) according to current guidelines
boolean
C3146298 (UMLS CUI [1,1])
C0021107 (UMLS CUI [1,2])
C0993733 (UMLS CUI [1,3])
C0033144 (UMLS CUI [1,4])
C3146298 (UMLS CUI [2,1])
C0021107 (UMLS CUI [2,2])
C0993733 (UMLS CUI [2,3])
C0679699 (UMLS CUI [2,4])
C0021107 (UMLS CUI [1,2])
C0993733 (UMLS CUI [1,3])
C0033144 (UMLS CUI [1,4])
C3146298 (UMLS CUI [2,1])
C0021107 (UMLS CUI [2,2])
C0993733 (UMLS CUI [2,3])
C0679699 (UMLS CUI [2,4])
Implantation Single chamber cardioverter-defibrillator Specified
Item
implanted with a biotronik lumax 540 vr-t dx icd with linoxsmart s dx or successor single chamber dx system within 90 days prior to enrollment
boolean
C0021107 (UMLS CUI [1,1])
C0993733 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
C0993733 (UMLS CUI [1,2])
C0205369 (UMLS CUI [1,3])
Informed Consent | Protocol Compliance
Item
written informed consent, willingness and ability to comply with the protocol
boolean
C0021430 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
C0525058 (UMLS CUI [2])
Age
Item
age < 18 years
boolean
C0001779 (UMLS CUI [1])
Contract Capability Limited
Item
any limitation to contractual capability
boolean
C0332522 (UMLS CUI [1,1])
C2698977 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
C2698977 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
female patients who are pregnant or breast feeding or plan a pregnancy during the course of the study
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Malignant Neoplasms | Malignant Neoplasms Patient recovered
Item
known active malignant disease or recovered from malignant disease within 2 years prior to enrollment
boolean
C0006826 (UMLS CUI [1])
C0006826 (UMLS CUI [2,1])
C1115804 (UMLS CUI [2,2])
C0006826 (UMLS CUI [2,1])
C1115804 (UMLS CUI [2,2])
Study Subject Participation Status
Item
simultaneous participation in another study
boolean
C2348568 (UMLS CUI [1])
Life Expectancy
Item
life expectancy < 2 years
boolean
C0023671 (UMLS CUI [1])