Informatie:
Fout:
ID
29481
Beschrijving
A Study of Triple-site Ventricular Pacing in Patients Who Have Not Responded to Conventional Dual Ventricular Site Cardiac Resynchronization Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT00941850
Link
https://clinicaltrials.gov/show/NCT00941850
Trefwoorden
Versies (2)
- 03-04-18 03-04-18 -
- 03-04-18 03-04-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
3 april 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Heart Failure NCT00941850
Eligibility Heart Failure NCT00941850
- StudyEvent: Eligibility
Similar models
Eligibility Heart Failure NCT00941850
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Implantation of CRT-D
Item
implanted with a crt device > 6 months previously according to current and conventional crt indications
boolean
C1135480 (UMLS CUI [1])
Medical Device Optimization
Item
device optimization > 1 months previously
boolean
C0025080 (UMLS CUI [1,1])
C2698650 (UMLS CUI [1,2])
C2698650 (UMLS CUI [1,2])
Age
Item
aged 18yrs or older
boolean
C0001779 (UMLS CUI [1])
Outpatient Follow-up Able
Item
able to attend outpatient follow up
boolean
C0029921 (UMLS CUI [1,1])
C3274571 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
C3274571 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
Myocardial Infarction
Item
recent mi (<2 months)
boolean
C0027051 (UMLS CUI [1])
Pregnancy | Pregnancy, Planned
Item
women who are pregnant or planning pregnancy
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
C0032992 (UMLS CUI [2])
Comorbidity Severe | Life Expectancy
Item
severe co morbid illness (where patients are not expected to survive duration of follow up period or where repeated outpatient visits may not be in best interest of patients)
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0023671 (UMLS CUI [2])
C0205082 (UMLS CUI [1,2])
C0023671 (UMLS CUI [2])
Medical contraindication Upgrade
Item
upgrade procedure is contraindicated for safety reasons.
boolean
C1301624 (UMLS CUI [1,1])
C3272274 (UMLS CUI [1,2])
C3272274 (UMLS CUI [1,2])
Inotropic agent Class
Item
class iv inotropic agents
boolean
C0304509 (UMLS CUI [1,1])
C0456387 (UMLS CUI [1,2])
C0456387 (UMLS CUI [1,2])
Protocol Compliance Unwilling
Item
patient unwilling to comply with required follow-up protocol including randomization scheme
boolean
C0525058 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
C0558080 (UMLS CUI [1,2])