Informationen:
Fehler:
ID
25803
Beschreibung
Testing Strategies to Improving Warfarin Adherence; ODM derived from: https://clinicaltrials.gov/show/NCT00622102
Link
https://clinicaltrials.gov/show/NCT00622102
Stichworte
Versionen (1)
- 20.09.17 20.09.17 -
Hochgeladen am
20. September 2017
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Atrial Fibrillation NCT00622102
Eligibility Atrial Fibrillation NCT00622102
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Atrial Fibrillation NCT00622102
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Age
Item
21 years old age or older
boolean
C0001779 (UMLS CUI [1])
on warfarin
Item
on warfarin managed at the ac clinic
boolean
C0851145 (UMLS CUI [1])
Target international normalized ratio
Item
target inr 2.0-3.0 or 2.5-3.5
boolean
C1272307 (UMLS CUI [1])
Therapeutic procedure Maintenance Phase | INR Stable | Warfarin Dosage Stable
Item
at maintenance phase of therapy (defined as stable inr with stable warfarin dosing over at least 2 consecutive visits)
boolean
C0087111 (UMLS CUI [1,1])
C0024501 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
C0525032 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
C0043031 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
C0205360 (UMLS CUI [3,3])
C0024501 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
C0525032 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
C0043031 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
C0205360 (UMLS CUI [3,3])
Access to telephone Lacking
Item
do not have access to telephone line
boolean
C1822200 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,2])
Study Subject Participation Status Unwilling | Informed Consent Refused
Item
unwillingness to participate or to sign a consent form(refusal)
boolean
C2348568 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
C0558080 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
Study Subject Participation Status Unable | Dementia Advanced | Alzheimer's Disease Advanced | Impairment Affecting Informed Consent | Impairment Affecting Data Quality | Impairment Affecting Medical care
Item
inability to participate because of advances dementia, advanced alzheimer's disease or other impairment affecting ability to provide informed consent and/or quality data or utilize the med-emonitor
boolean
C2348568 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0497327 (UMLS CUI [2,1])
C0205179 (UMLS CUI [2,2])
C0002395 (UMLS CUI [3,1])
C0205179 (UMLS CUI [3,2])
C0221099 (UMLS CUI [4,1])
C0392760 (UMLS CUI [4,2])
C0021430 (UMLS CUI [4,3])
C0221099 (UMLS CUI [5,1])
C0392760 (UMLS CUI [5,2])
C0242483 (UMLS CUI [5,3])
C0221099 (UMLS CUI [6,1])
C0392760 (UMLS CUI [6,2])
C0496675 (UMLS CUI [6,3])
C1299582 (UMLS CUI [1,2])
C0497327 (UMLS CUI [2,1])
C0205179 (UMLS CUI [2,2])
C0002395 (UMLS CUI [3,1])
C0205179 (UMLS CUI [3,2])
C0221099 (UMLS CUI [4,1])
C0392760 (UMLS CUI [4,2])
C0021430 (UMLS CUI [4,3])
C0221099 (UMLS CUI [5,1])
C0392760 (UMLS CUI [5,2])
C0242483 (UMLS CUI [5,3])
C0221099 (UMLS CUI [6,1])
C0392760 (UMLS CUI [6,2])
C0496675 (UMLS CUI [6,3])
Study Subject Participation Status Illicit
Item
participation in a current study that does not permit participation in another study
boolean
C2348568 (UMLS CUI [1,1])
C0332266 (UMLS CUI [1,2])
C0332266 (UMLS CUI [1,2])
Terminal illness | Life Expectancy
Item
end stage or terminal illness with anticipated life expectancy of 6 months or less
boolean
C0679247 (UMLS CUI [1])
C0023671 (UMLS CUI [2])
C0023671 (UMLS CUI [2])
INR raised
Item
inr over the upper limit for the individual's range at the time of enrollment (e.g.,>3.0 or >3.5, depending on the target range)
boolean
C0853225 (UMLS CUI [1])
Antiphospholipid Syndrome | INR abnormal
Item
diagnosed with antiphospholipid antibody syndrome or abnormal inr prior to starting warfarin
boolean
C0085278 (UMLS CUI [1])
C0580417 (UMLS CUI [2])
C0580417 (UMLS CUI [2])