Informationen:
Fehler:
ID
28383
Beschreibung
Post Approval Registry of Corox OTW, Endocardial, Left Ventricular Steroid Lead, Bipolar; ODM derived from: https://clinicaltrials.gov/show/NCT00810264
Link
https://clinicaltrials.gov/show/NCT00810264
Stichworte
Versionen (1)
- 09.01.18 09.01.18 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
9. Januar 2018
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY 4.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Congestive Heart Failure NCT00810264
Eligibility Congestive Heart Failure NCT00810264
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Congestive Heart Failure NCT00810264
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Cardiac Resynchronization Therapy Device Implantation Successful | Other Coding
Item
successfully implanted biotronik crt system, including a corox bp lv lead, from 7-180 days prior to enrollment
boolean
C2936377 (UMLS CUI [1,1])
C0021107 (UMLS CUI [1,2])
C1272703 (UMLS CUI [1,3])
C3846158 (UMLS CUI [2])
C0021107 (UMLS CUI [1,2])
C1272703 (UMLS CUI [1,3])
C3846158 (UMLS CUI [2])
Comprehension Enrollment | Informed Consent
Item
able to understand the nature of the registry and give informed consent
boolean
C0162340 (UMLS CUI [1,1])
C1516879 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
C1516879 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
Patient Available Follow-up visit
Item
available for follow-up visits on a regular basis at the investigational site
boolean
C0030705 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C0589121 (UMLS CUI [1,3])
C0470187 (UMLS CUI [1,2])
C0589121 (UMLS CUI [1,3])
Age
Item
age greater than or equal to 18 years
boolean
C0001779 (UMLS CUI [1])
Study Subject Participation Status | IDE Clinical Trial
Item
enrolled in any ide clinical study
boolean
C2348568 (UMLS CUI [1])
C2826366 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C2826366 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
Cardiac Surgery procedures Planned | Interventional procedure Planned
Item
planned cardiac surgical procedures or interventional measures within the next 6 months
boolean
C0018821 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0184661 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
C1301732 (UMLS CUI [1,2])
C0184661 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
Heart Transplantation Expected
Item
expected to receive a heart transplant within 1 year
boolean
C0018823 (UMLS CUI [1,1])
C1517001 (UMLS CUI [1,2])
C1517001 (UMLS CUI [1,2])
Life Expectancy
Item
life expectancy less than 1 year
boolean
C0023671 (UMLS CUI [1])
Comorbidity Life Threatening | Independent of Heart Disease
Item
presence of another life-threatening, underlying illness separate from their cardiac disorder
boolean
C0009488 (UMLS CUI [1,1])
C2826244 (UMLS CUI [1,2])
C0332291 (UMLS CUI [2,1])
C0018799 (UMLS CUI [2,2])
C2826244 (UMLS CUI [1,2])
C0332291 (UMLS CUI [2,1])
C0018799 (UMLS CUI [2,2])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Protocol Compliance Unable | Implant Date No Information Available | Device implant No Information Available | Age No Information Available | Gender No Information Available | Adverse event No Information Available
Item
inability to provide date of implant, devices implanted, age, gender, and whether the patient experienced any protocol-defined adverse events since implant
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021107 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C1546437 (UMLS CUI [2,3])
C0948629 (UMLS CUI [3,1])
C1546437 (UMLS CUI [3,2])
C0001779 (UMLS CUI [4,1])
C1546437 (UMLS CUI [4,2])
C0079399 (UMLS CUI [5,1])
C1546437 (UMLS CUI [5,2])
C0877248 (UMLS CUI [6,1])
C1546437 (UMLS CUI [6,2])
C1299582 (UMLS CUI [1,2])
C0021107 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C1546437 (UMLS CUI [2,3])
C0948629 (UMLS CUI [3,1])
C1546437 (UMLS CUI [3,2])
C0001779 (UMLS CUI [4,1])
C1546437 (UMLS CUI [4,2])
C0079399 (UMLS CUI [5,1])
C1546437 (UMLS CUI [5,2])
C0877248 (UMLS CUI [6,1])
C1546437 (UMLS CUI [6,2])