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Informatie:
Fout:
ID
39993
Beschrijving
Renal Denervation in Patients With Uncontrolled Hypertension in Chinese; ODM derived from: https://clinicaltrials.gov/show/NCT01390831
Link
https://clinicaltrials.gov/show/NCT01390831
Trefwoorden
Versies (2)
- 08-03-20 08-03-20 -
- 09-03-20 09-03-20 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
8 maart 2020
DOI
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Licentie
Creative Commons BY-NC 4.0
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Eligibility Hypertension NCT01390831
Eligibility Hypertension NCT01390831
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT01390831
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
>= 18 years of age
boolean
C0001779 (UMLS CUI [1])
Systolic Pressure | Diastolic blood pressure
Item
a systolic blood pressure of 160mmhg or more and/or a diastolic blood pressure of 90mmhg or more
boolean
C0871470 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
C0428883 (UMLS CUI [2])
Antihypertensive therapy Quantity Dose Full
Item
receiving and adhering to at least three full doses of appropriate antihypertensive drug regimen
boolean
C0585941 (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])
Secondary hypertension
Item
secondary hypertension
boolean
C0155616 (UMLS CUI [1])
Abnormal renal artery morphology
Item
renal arterial abnormalities
boolean
C4024624 (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])
Implantable defibrillator | Artificial cardiac pacemaker | Metallic implant Inconsistent Magnetic Resonance Imaging
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])
C0442809 (UMLS CUI [3,2])
C0024485 (UMLS CUI [3,3])
C0030163 (UMLS CUI [2])
C3693688 (UMLS CUI [3,1])
C0442809 (UMLS CUI [3,2])
C0024485 (UMLS CUI [3,3])
Requirement Support respiratory
Item
requires respiratory support
boolean
C1514873 (UMLS CUI [1,1])
C1521721 (UMLS CUI [1,2])
C0521346 (UMLS CUI [1,3])
C1521721 (UMLS CUI [1,2])
C0521346 (UMLS CUI [1,3])
Sick Sinus Syndrome
Item
patients with sick sinus syndrome
boolean
C0037052 (UMLS CUI [1])
Pregnancy
Item
pregnant woman
boolean
C0032961 (UMLS CUI [1])
Exclusion Criteria Additional
Item
others
boolean
C0680251 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])
C1524062 (UMLS CUI [1,2])