Informationen:
Fehler:
ID
23205
Beschreibung
Blood Pressure Lowering Ability and Safety of an Olmesartan and Amlodipine Based Treatment Regimen in Patients With Stage I and Stage II Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00527514
Link
https://clinicaltrials.gov/show/NCT00527514
Stichworte
Versionen (1)
- 28.06.17 28.06.17 -
Hochgeladen am
28. Juni 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 Hypertension NCT00527514
Eligibility Hypertension NCT00527514
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Hypertension NCT00527514
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
ID.1
Item
males or females greater than or equal to 18 years of age
boolean
C0001779 (UMLS CUI [1])
ID.2
Item
patients with a mean seated systolic blood pressure (mssbp) greater than or equal to 140 mm hg but less than or equal to 199 mm hg or a mean seated diastolic blood pressure (msdbp) greater than or equal to 90 mm hg and less than or equal to 109 mm hg, following a period of taking only placebo
boolean
C0005823 (UMLS CUI [1,1])
C0420256 (UMLS CUI [1,2])
C0420256 (UMLS CUI [1,2])
ID.3
Item
patients with a mean daytime (8am-4pm) systolic blood pressure greater than or equal to 135 mm hg and less than or equal to 199 mm hg and a mean daytime diastolic blood pressure less than or equal to 109 mm hg as measured by an ambulatory blood pressure monitoring device (abpm), after a period of taking only placebo
boolean
C0005823 (UMLS CUI [1,1])
C0420256 (UMLS CUI [1,2])
C0420256 (UMLS CUI [1,2])
ID.4
Item
if female, must have negative serum pregnancy test at screening and be either post-menopausal (greater than or equal to 1 year), had a hysterectomy or tubal ligation at least 6 months before consent or if of childbearing potential, must practice approved measures of birth control throughout study
boolean
C0032961 (UMLS CUI [1,1])
C0009862 (UMLS CUI [1,2])
C0232970 (UMLS CUI [1,3])
C0009862 (UMLS CUI [1,2])
C0232970 (UMLS CUI [1,3])
ID.5
Item
history of stroke or transient ischemic attack (tia) within the last one year
boolean
C0038454 (UMLS CUI [1,1])
C0007787 (UMLS CUI [1,2])
C0007787 (UMLS CUI [1,2])
ID.6
Item
history of myocardial infarction, coronary angioplasty, coronary artery bypass graft, or heart failure within the past 6 months
boolean
C0027051 (UMLS CUI [1,1])
C0190211 (UMLS CUI [1,2])
C0396750 (UMLS CUI [1,3])
C0018801 (UMLS CUI [1,4])
C0190211 (UMLS CUI [1,2])
C0396750 (UMLS CUI [1,3])
C0018801 (UMLS CUI [1,4])
ID.7
Item
patients with secondary hypertension of any etiology, such as renal disease, pheochromocytoma, or cushing's syndrome
boolean
C0155616 (UMLS CUI [1])
ID.8
Item
type i diabetes. patients with type ii diabetes on stable treatment, with fasting glucose <160 mg/dl may enroll
boolean
C0011854 (UMLS CUI [1])
ID.9
Item
patients with hemodynamically significant cardiac valvular disease
boolean
C0018824 (UMLS CUI [1,1])
C0948268 (UMLS CUI [1,2])
C0948268 (UMLS CUI [1,2])
ID.10
Item
patients with clinically significant cardiac conduction defects, including second or third degree av block, left bundle branch block, sick sinus syndrome, atrial fibrillation, atrial flutter, an accessory bypass tract, or any arrhythmia requiring medication
boolean
C0018799 (UMLS CUI [1])