ID

24417

Beschreibung

Renal Denervation in Patients With Refractory Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00483808

Link

https://clinicaltrials.gov/show/NCT00483808

Stichworte

  1. 31.07.17 31.07.17 -
Hochgeladen am

31. Juli 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 NCT00483808

Eligibility Hypertension NCT00483808

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
>= 18 years of age.
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
a systolic blood pressure of 160 mmhg or greater.
Beschreibung

Systolic Pressure

Datentyp

boolean

Alias
UMLS CUI [1]
C0871470
receiving and adhering to full doses of an appropriate antihypertensive drug regimen for a minimum of two weeks prior to screening.
Beschreibung

Antihypertensive Agents Dose Full

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0443225
agrees to have the study procedure(s) performed and additional procedures and evaluations, including repeat phlebotomy, imaging, urine analyses, and clinical examination.
Beschreibung

Protocol Compliance | Venesection Repeated | Imaging | Urinalysis | examination; clinical

Datentyp

boolean

Alias
UMLS CUI [1]
C0525058
UMLS CUI [2,1]
C0684257
UMLS CUI [2,2]
C0205341
UMLS CUI [3]
C0011923
UMLS CUI [4]
C0042014
UMLS CUI [5]
C1456356
competent and willing to provide written, informed consent to participate in this clinical study.
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
renal arterial abnormalities
Beschreibung

Renal artery Abnormality

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0035065
UMLS CUI [1,2]
C1704258
end stage renal disease requiring dialysis or renal transplant
Beschreibung

Chronic Kidney Failure Requirement Dialysis | Chronic Kidney Failure Requirement Kidney Transplantation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0022661
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0011946
UMLS CUI [2,1]
C0022661
UMLS CUI [2,2]
C1514873
UMLS CUI [2,3]
C0022671
serum cr > 3, or calculated gfr < 45 ml/min
Beschreibung

Creatinine measurement, serum | Estimated Glomerular Filtration Rate

Datentyp

boolean

Alias
UMLS CUI [1]
C0201976
UMLS CUI [2]
C3811844
has experienced mi, unstable angina pectoris, or cva with 6 months
Beschreibung

Myocardial Infarction | Angina, Unstable | Cerebrovascular accident

Datentyp

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0002965
UMLS CUI [3]
C0038454
others
Beschreibung

Exclusion Criteria Additional

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0680251
UMLS CUI [1,2]
C1524062

Ähnliche Modelle

Eligibility Hypertension NCT00483808

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
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])
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])
Informed Consent
Item
competent and willing to provide written, informed consent to participate in this clinical study.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Renal artery Abnormality
Item
renal arterial abnormalities
boolean
C0035065 (UMLS CUI [1,1])
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])
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])
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])
Exclusion Criteria Additional
Item
others
boolean
C0680251 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video