Informazione:
Errore:
ID
29935
Descrizione
Renal Denervation in Patients With Refractory Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00664638
collegamento
https://clinicaltrials.gov/show/NCT00664638
Keywords
versioni (1)
- 27/04/18 27/04/18 -
Titolare del copyright
See clinicaltrials.gov
Caricato su
27 aprile 2018
DOI
Per favore, per richiedere un accesso.
Licenza
Creative Commons BY 4.0
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Eligibility Hypertension NCT00664638
Eligibility Hypertension NCT00664638
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT00664638
- StudyEvent: Eligibility
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Age
Item
>= 18 years of age
boolean
C0001779 (UMLS CUI [1])
Systolic Pressure
Item
a systolic blood pressure of 160mmhg or more
boolean
C0871470 (UMLS CUI [1])
Antihypertensive Agents Quantity Dose Full
Item
receiving and adhering to full doses of at least three antihypertensive drugs
boolean
C0003364 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0443225 (UMLS CUI [1,4])
C1265611 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0443225 (UMLS CUI [1,4])
Estimated Glomerular Filtration Rate
Item
estimated glomerular filtration rate (egfr) of ≥45ml/min
boolean
C3811844 (UMLS CUI [1])
Protocol Compliance
Item
agrees to have the study procedure(s) performed and additional procedures and evaluations
boolean
C0525058 (UMLS CUI [1])
Informed Consent
Item
is competent and willing to provide written, informed consent to participate in this clinical study
boolean
C0021430 (UMLS CUI [1])
Renal Artery Stenosis
Item
hemodynamically or anatomically significant renal artery stenosis
boolean
C0035067 (UMLS CUI [1])
Angioplasty renal artery
Item
has a history or prior renal artery angioplasty
boolean
C1282893 (UMLS CUI [1])
Myocardial Infarction | Angina, Unstable | Cerebrovascular accident
Item
has experienced mi, unstable angina pectoris, or cva within 6 months
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0002965 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
Heart valve disease
Item
has hemodynamically significant valvular heart disease
boolean
C0018824 (UMLS CUI [1])
Diabetes Mellitus, Insulin-Dependent
Item
has type 1 diabetes
boolean
C0011854 (UMLS CUI [1])
Implantable defibrillator | Artificial cardiac pacemaker | Metallic implant Incompatibility Problem MRI
Item
has an implantable cardioverter defibrillator (icd) or pacemaker, or any other metallic implant which is not compatible with magnetic resonance imaging (mri)
boolean
C0162589 (UMLS CUI [1])
C0030163 (UMLS CUI [2])
C3693688 (UMLS CUI [3,1])
C1881693 (UMLS CUI [3,2])
C0024485 (UMLS CUI [3,3])
C0030163 (UMLS CUI [2])
C3693688 (UMLS CUI [3,1])
C1881693 (UMLS CUI [3,2])
C0024485 (UMLS CUI [3,3])
Patient need for Support respiratory
Item
requires respiratory support
boolean
C0686904 (UMLS CUI [1,1])
C0344211 (UMLS CUI [1,2])
C0521346 (UMLS CUI [1,3])
C0344211 (UMLS CUI [1,2])
C0521346 (UMLS CUI [1,3])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
is pregnant, nursing, or planning to be pregnant
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Drug usage | Alcoholic Intoxication, Chronic
Item
has known, unresolved history of drug use or alcohol dependency.
boolean
C0242510 (UMLS CUI [1])
C0001973 (UMLS CUI [2])
C0001973 (UMLS CUI [2])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
is currently enrolled in another investigational drug or device trial.
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])