Informatie:
Fout:
ID
19773
Beschrijving
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
Trefwoorden
Versies (1)
- 27-01-17 27-01-17 -
Geüploaded op
27 januari 2017
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility Cardiovascular Disease NCT00334724
Eligibility Cardiovascular Disease NCT00334724
- StudyEvent: Eligibility
Similar models
Eligibility Cardiovascular Disease NCT00334724
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])