Eligibility Hypertension NCT01119417

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with autonomic failure and supine hypertension from all races, who are in the hospital participating in the study "the evaluation and treatment of autonomic failure" (irb# 000814).
Beschrijving

ID.1

Datatype

boolean

supine hypertension, defined as a systolic blood pressure >150 mm hg or diastolic blood pressure > 90 mm hg.
Beschrijving

ID.2

Datatype

boolean

males and females, between 18-85yr.
Beschrijving

ID.3

Datatype

boolean

provide written informed consent to participate in the study and understand that they may withdraw their consent at any time without prejudice to their future medical care.
Beschrijving

ID.4

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant women.
Beschrijving

ID.5

Datatype

boolean

high-risk patients (e.g. heart failure, symptomatic coronary artery disease, liver impairment, history of stroke or myocardial infarction).
Beschrijving

ID.6

Datatype

boolean

history of serious allergies or asthma.
Beschrijving

ID.7

Datatype

boolean

in the investigator's opinion, have clinically significant abnormalities on clinical, mental examination or laboratory testing.
Beschrijving

ID.8

Datatype

boolean

all medical students.
Beschrijving

ID.9

Datatype

boolean

Similar models

Eligibility Hypertension NCT01119417

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
patients with autonomic failure and supine hypertension from all races, who are in the hospital participating in the study "the evaluation and treatment of autonomic failure" (irb# 000814).
boolean
ID.2
Item
supine hypertension, defined as a systolic blood pressure >150 mm hg or diastolic blood pressure > 90 mm hg.
boolean
ID.3
Item
males and females, between 18-85yr.
boolean
ID.4
Item
provide written informed consent to participate in the study and understand that they may withdraw their consent at any time without prejudice to their future medical care.
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
pregnant women.
boolean
ID.6
Item
high-risk patients (e.g. heart failure, symptomatic coronary artery disease, liver impairment, history of stroke or myocardial infarction).
boolean
ID.7
Item
history of serious allergies or asthma.
boolean
ID.8
Item
in the investigator's opinion, have clinically significant abnormalities on clinical, mental examination or laboratory testing.
boolean
ID.9
Item
all medical students.
boolean