Informationen:
Fehler:
ID
27583
Beschreibung
Differential Intervention Trial by Standard Therapy Versus Pitavastatin in Patients With Chronic Hemodialysis (DIALYSIS); ODM derived from: https://clinicaltrials.gov/show/NCT00846118
Link
https://clinicaltrials.gov/show/NCT00846118
Stichworte
Versionen (1)
- 21.11.17 21.11.17 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
21. November 2017
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 Cardiovascular Disease NCT00846118
Eligibility Cardiovascular Disease NCT00846118
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Cardiovascular Disease NCT00846118
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Hemodialysis
Item
patients under hemodialysis
boolean
C0019004 (UMLS CUI [1])
Hypercholesterolemia
Item
patients with hypercholesterolemia as defined by any of following parameters:
boolean
C0020443 (UMLS CUI [1])
Low density lipoprotein cholesterol measurement
Item
ldl-c ≧ 100 mg / dl
boolean
C0202117 (UMLS CUI [1])
Serum total cholesterol measurement
Item
tc ≧ 180 mg / dl
boolean
C1445957 (UMLS CUI [1])
Anticholesteremic Agents Patient need for
Item
patients required cholesterol-lowering treatment by investigators.
boolean
C0003277 (UMLS CUI [1,1])
C0686904 (UMLS CUI [1,2])
C0686904 (UMLS CUI [1,2])
Age
Item
patients aged 20-75 years
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
patients with written consent by their own volition after being provided sufficient explanation for the participation into this clinical trial
boolean
C0021430 (UMLS CUI [1])
Statins | Fibrates
Item
patients taking statins or fibrates
boolean
C0360714 (UMLS CUI [1])
C1449704 (UMLS CUI [2])
C1449704 (UMLS CUI [2])
Study Subject Participation Status | Medical contraindication pitavastatin
Item
patients enrolled to the other trials using contraindication drugs of pitavastatin
boolean
C2348568 (UMLS CUI [1])
C1301624 (UMLS CUI [2,1])
C1101838 (UMLS CUI [2,2])
C1301624 (UMLS CUI [2,1])
C1101838 (UMLS CUI [2,2])
Myocardial Infarction
Item
patients who had acute myocardial infarction within six months before the day of the agreement acquisition
boolean
C0027051 (UMLS CUI [1])
Percutaneous Coronary Intervention Scheduled | Coronary Artery Bypass Surgery Scheduled
Item
patients scheduled pci and cabg within six months after the day of the agreement acquisition
boolean
C1532338 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
C0010055 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
C0205539 (UMLS CUI [1,2])
C0010055 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
Malignant Neoplasms | Malignant Neoplasms Unlikely
Item
patients who had diagnosis or doubt of malignant tumor
boolean
C0006826 (UMLS CUI [1])
C0006826 (UMLS CUI [2,1])
C0750558 (UMLS CUI [2,2])
C0006826 (UMLS CUI [2,1])
C0750558 (UMLS CUI [2,2])
Medical contraindication pitavastatin
Item
patients corresponded to "contraindications" of pitavastatin
boolean
C1301624 (UMLS CUI [1,1])
C1101838 (UMLS CUI [1,2])
C1101838 (UMLS CUI [1,2])
Hypercholesterolemia, Familial
Item
familial hypercholesterolemia patients
boolean
C0020445 (UMLS CUI [1])
Patients Ineligible
Item
patients judged ineligible by investigators
boolean
C0030705 (UMLS CUI [1,1])
C1512714 (UMLS CUI [1,2])
C1512714 (UMLS CUI [1,2])