Information:
Fel:
ID
43985
Beskrivning
A Study of the Effect of Nebivolol to Evaluate Its Vasodilatory Effects in Hypertensive Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00648895
Länk
https://clinicaltrials.gov/show/NCT00648895
Nyckelord
Versioner (2)
- 2017-08-01 2017-08-01 -
- 2021-09-20 2021-09-20 -
Uppladdad den
20 september 2021
DOI
För en begäran logga in.
Licens
Creative Commons BY 4.0
Modellkommentarer :
Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.
Itemgroup-kommentar för :
Item-kommentar för :
Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.
Eligibility Hypertension NCT00648895
Eligibility Hypertension NCT00648895
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT00648895
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Outpatients Ambulatory | Age
Item
male or female, ambulatory outpatients 18-79 years old at screening
boolean
C0029921 (UMLS CUI [1,1])
C1561561 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
C1561561 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
Hypertensive disease Stage Disease length
Item
minimum 2-year history of stage i/ii hypertension
boolean
C0020538 (UMLS CUI [1,1])
C1306673 (UMLS CUI [1,2])
C0872146 (UMLS CUI [1,3])
C1306673 (UMLS CUI [1,2])
C0872146 (UMLS CUI [1,3])
Blood pressure measurement
Item
qualifying blood pressure criteria for study entry and for randomization
boolean
C0005824 (UMLS CUI [1])
Compliance behavior Dietary | Protocol Compliance
Item
willing to adhere to the dietary compliance and undergo protocol procedures
boolean
C1321605 (UMLS CUI [1,1])
C0012155 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2])
C0012155 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2])
Life Style allowing Evaluation
Item
have a lifestyle that will permit him/her to attend all evaluations, including those conducted on consecutive days
boolean
C0023676 (UMLS CUI [1,1])
C0683607 (UMLS CUI [1,2])
C1261322 (UMLS CUI [1,3])
C0683607 (UMLS CUI [1,2])
C1261322 (UMLS CUI [1,3])
Secondary hypertension
Item
have any form of secondary hypertension
boolean
C0155616 (UMLS CUI [1])
Respiration Disorders | Cardiovascular Diseases
Item
have clinically significant respiratory or cardiovascular disease
boolean
C0035204 (UMLS CUI [1])
C0007222 (UMLS CUI [2])
C0007222 (UMLS CUI [2])
Coronary Artery Disease | Peripheral Vascular Diseases
Item
presence/history of coronary artery disease or peripheral vascular disease
boolean
C1956346 (UMLS CUI [1])
C0085096 (UMLS CUI [2])
C0085096 (UMLS CUI [2])
Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent
Item
have diabetes mellitus, type i or ii
boolean
C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
C0011860 (UMLS CUI [2])
Hypersensitivity nebivolol | Metoprolol allergy | BETA BLOCKER ALLERGY
Item
have a history of hypersensitivity to nebivolol, metoprolol, or any beta-blocker
boolean
C0020517 (UMLS CUI [1,1])
C0068475 (UMLS CUI [1,2])
C0570889 (UMLS CUI [2])
C0741466 (UMLS CUI [3])
C0068475 (UMLS CUI [1,2])
C0570889 (UMLS CUI [2])
C0741466 (UMLS CUI [3])