Informationen:
Fehler:
ID
19773
Beschreibung
Home Blood Pressure-guided Antihypertensive Intervention for Elderly (HBP-GUIDE) Study; ODM derived from: https://clinicaltrials.gov/show/NCT00334724
Link
https://clinicaltrials.gov/show/NCT00334724
Stichworte
Versionen (1)
- 27.01.17 27.01.17 -
Hochgeladen am
27. Januar 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 NCT00334724
Eligibility Cardiovascular Disease NCT00334724
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Cardiovascular Disease NCT00334724
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Outpatients | Age
Item
outpatients aged over 65 years and less than 80 years
boolean
C0029921 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0001779 (UMLS CUI [2])
Systolic Pressure Stable | Diastolic blood pressure Stable
Item
patients with a stable seated systolic blood pressure of ≥ 140 mmhg or diastolic blood pressure of ≥ 90 mmhg at two visits within 8 weeks
boolean
C0871470 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0428883 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
C0205360 (UMLS CUI [1,2])
C0428883 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
Average home systolic blood pressure | Average home diastolic blood pressure
Item
patients with a stable seated systolic blood pressure of ≥ 135 mmhg or diastolic blood pressure of ≥ 85 mmhg at home (home blood pressure is measured every morning within 1 h of waking, and defined as the mean of 3 days measurement within 8 weeks)
boolean
C1531726 (UMLS CUI [1])
C1531725 (UMLS CUI [2])
C1531725 (UMLS CUI [2])
Secondary hypertension | Malignant Hypertension
Item
patients with secondary hypertension or malignant hypertension
boolean
C0155616 (UMLS CUI [1])
C0020540 (UMLS CUI [2])
C0020540 (UMLS CUI [2])
Systolic Pressure Stable | Diastolic blood pressure Stable
Item
patients with a stable seated systolic pressure of ≥ 180 mmhg or diastolic pressure of ≥ 110 mmhg
boolean
C0871470 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0428883 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
C0205360 (UMLS CUI [1,2])
C0428883 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
Renal dysfunction | Creatinine measurement, serum
Item
patients with renal dysfunction with a serum creatinine level of ≥ 2 mg/dl
boolean
C3279454 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C0201976 (UMLS CUI [2])
Liver Dysfunction
Item
patients with liver dysfunction
boolean
C0086565 (UMLS CUI [1])
Hypersensitivity Angiotensin II receptor antagonist
Item
patients with a history of hypersensitivity to angiotensin ii receptor blockade
boolean
C0020517 (UMLS CUI [1,1])
C0521942 (UMLS CUI [1,2])
C0521942 (UMLS CUI [1,2])
Myocardial Infarction
Item
patients with a history of myocardial infarction within 6 months prior to enrolment in the study
boolean
C0027051 (UMLS CUI [1])
Coronary angioplasty
Item
patients who underwent coronary arterioplasty within 6 months prior to enrolment in the study or patients who will undergo coronary arterioplasty within 6 months after entry
boolean
C0190211 (UMLS CUI [1])
Heart failure
Item
patients with heart failure
boolean
C0018801 (UMLS CUI [1])
Cerebrovascular Disorders
Item
patients with a history of cerebrovascular disorder
boolean
C0007820 (UMLS CUI [1])
Patients Inappropriate Clinical Trial
Item
other patients who are judged to be inappropriate for the study by the investigator
boolean
C0030705 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C1548788 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])