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ID
24417
Beschrijving
Renal Denervation in Patients With Refractory Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00483808
Link
https://clinicaltrials.gov/show/NCT00483808
Trefwoorden
Versies (1)
- 31-07-17 31-07-17 -
Geüploaded op
31 juli 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Hypertension NCT00483808
Eligibility Hypertension NCT00483808
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT00483808
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
>= 18 years of age.
boolean
C0001779 (UMLS CUI [1])
Systolic Pressure
Item
a systolic blood pressure of 160 mmhg or greater.
boolean
C0871470 (UMLS CUI [1])
Antihypertensive Agents Dose Full
Item
receiving and adhering to full doses of an appropriate antihypertensive drug regimen for a minimum of two weeks prior to screening.
boolean
C0003364 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0443225 (UMLS CUI [1,3])
C0178602 (UMLS CUI [1,2])
C0443225 (UMLS CUI [1,3])
Protocol Compliance | Venesection Repeated | Imaging | Urinalysis | examination; clinical
Item
agrees to have the study procedure(s) performed and additional procedures and evaluations, including repeat phlebotomy, imaging, urine analyses, and clinical examination.
boolean
C0525058 (UMLS CUI [1])
C0684257 (UMLS CUI [2,1])
C0205341 (UMLS CUI [2,2])
C0011923 (UMLS CUI [3])
C0042014 (UMLS CUI [4])
C1456356 (UMLS CUI [5])
C0684257 (UMLS CUI [2,1])
C0205341 (UMLS CUI [2,2])
C0011923 (UMLS CUI [3])
C0042014 (UMLS CUI [4])
C1456356 (UMLS CUI [5])
Informed Consent
Item
competent and willing to provide written, informed consent to participate in this clinical study.
boolean
C0021430 (UMLS CUI [1])
Renal artery Abnormality
Item
renal arterial abnormalities
boolean
C0035065 (UMLS CUI [1,1])
C1704258 (UMLS CUI [1,2])
C1704258 (UMLS CUI [1,2])
Chronic Kidney Failure Requirement Dialysis | Chronic Kidney Failure Requirement Kidney Transplantation
Item
end stage renal disease requiring dialysis or renal transplant
boolean
C0022661 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0011946 (UMLS CUI [1,3])
C0022661 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0022671 (UMLS CUI [2,3])
C1514873 (UMLS CUI [1,2])
C0011946 (UMLS CUI [1,3])
C0022661 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0022671 (UMLS CUI [2,3])
Creatinine measurement, serum | Estimated Glomerular Filtration Rate
Item
serum cr > 3, or calculated gfr < 45 ml/min
boolean
C0201976 (UMLS CUI [1])
C3811844 (UMLS CUI [2])
C3811844 (UMLS CUI [2])
Myocardial Infarction | Angina, Unstable | Cerebrovascular accident
Item
has experienced mi, unstable angina pectoris, or cva with 6 months
boolean
C0027051 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0002965 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
Exclusion Criteria Additional
Item
others
boolean
C0680251 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])
C1524062 (UMLS CUI [1,2])