ID

39978

Descrizione

Contribution of Angiotensin II to Supine Hypertension in Autonomic Failure; ODM derived from: https://clinicaltrials.gov/show/NCT01292694

collegamento

https://clinicaltrials.gov/show/NCT01292694

Keywords

versioni (1)
  1. 07/03/20 07/03/20 -
Titolare del copyright

See clinicaltrials.gov

Caricato su

7 marzo 2020

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY 4.0
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Eligibility Hypertension NCT01292694

Inglese

Eligibility Hypertension NCT01292694

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients with autonomic failure who exhibit supine hypertension and are in the hospital already participating in the study "the evaluation and treatment of autonomic failure [irb # 000814]
Descrizione

Autonomic Failure | Supine hypertension | Participation Clinical Trial Specified

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0393911
UMLS CUI [2]
C4076686
UMLS CUI [3,1]
C0679823
UMLS CUI [3,2]
C0008976
UMLS CUI [3,3]
C0205369
supine hypertension, defined as systolic blood pressure > 150 mm hg and/or diastolic blood pressure > 90 mm hg
Descrizione

Supine hypertension | Systolic Pressure | Diastolic blood pressure

Tipo di dati

boolean

Alias
UMLS CUI [1]
C4076686
UMLS CUI [2]
C0871470
UMLS CUI [3]
C0428883
males and females of all races, between 18 to 85 years of age
Descrizione

Racial group All | Age

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0034510
UMLS CUI [1,2]
C0444868
UMLS CUI [2]
C0001779
able and willing to provide informed consent with the understanding that they may withdraw consent at any time without prejudice to future medical care
Descrizione

Informed Consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
all medical students
Descrizione

Medical Students All

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0038495
UMLS CUI [1,2]
C0444868
pregnant women
Descrizione

Pregnancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
patients with a history of angioedema
Descrizione

Angioedema

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0002994
patients with a known allergy to any ace inhibitor or angiotensin receptor blocker
Descrizione

Angiotensin-converting-enzyme inhibitor allergy | Allergy to angiotensin II receptor antagonist

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0571939
UMLS CUI [2]
C2585204
high-risk patients [e.g. heart failure, symptomatic coronary artery disease, liver impairment, history of stroke or myocardial infarction]
Descrizione

High risk Patients | Heart failure | Coronary Artery Disease Symptomatic | Hepatic impairment | Cerebrovascular accident | Myocardial Infarction

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C4319571
UMLS CUI [1,2]
C0030705
UMLS CUI [2]
C0018801
UMLS CUI [3,1]
C1956346
UMLS CUI [3,2]
C0231220
UMLS CUI [4]
C0948807
UMLS CUI [5]
C0038454
UMLS CUI [6]
C0027051
patients with hemoglobin < 10.5 [or hematocrit < 32]
Descrizione

Hemoglobin measurement | Hematocrit measurement

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0518015
UMLS CUI [2]
C0018935
inability to give, or withdraw, informed consent
Descrizione

Informed Consent Unable | Informed Consent Withdrawn

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C2349954
other factors which in the investigator's opinion would prevent the patient from completing the protocol including clinically significant abnormalities in clinical, mental or laboratory testing
Descrizione

Factor Preventing Completion of clinical trial | Clinical Test Result Abnormal | Mental Tests Abnormal | Laboratory test result abnormal

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1521761
UMLS CUI [1,2]
C1292733
UMLS CUI [1,3]
C2732579
UMLS CUI [2,1]
C0456984
UMLS CUI [2,2]
C0205161
UMLS CUI [3,1]
C0025365
UMLS CUI [3,2]
C0205161
UMLS CUI [4]
C0438215
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Similar models

Eligibility Hypertension NCT01292694

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Autonomic Failure | Supine hypertension | Participation Clinical Trial Specified
Item
patients with autonomic failure who exhibit supine hypertension and are in the hospital already participating in the study "the evaluation and treatment of autonomic failure [irb # 000814]
boolean
C0393911 (UMLS CUI [1])
C4076686 (UMLS CUI [2])
C0679823 (UMLS CUI [3,1])
C0008976 (UMLS CUI [3,2])
C0205369 (UMLS CUI [3,3])
Supine hypertension | Systolic Pressure | Diastolic blood pressure
Item
supine hypertension, defined as systolic blood pressure > 150 mm hg and/or diastolic blood pressure > 90 mm hg
boolean
C4076686 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Racial group All | Age
Item
males and females of all races, between 18 to 85 years of age
boolean
C0034510 (UMLS CUI [1,1])
C0444868 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
Informed Consent
Item
able and willing to provide informed consent with the understanding that they may withdraw consent at any time without prejudice to future medical care
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Medical Students All
Item
all medical students
boolean
C0038495 (UMLS CUI [1,1])
C0444868 (UMLS CUI [1,2])
Pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
Angioedema
Item
patients with a history of angioedema
boolean
C0002994 (UMLS CUI [1])
Angiotensin-converting-enzyme inhibitor allergy | Allergy to angiotensin II receptor antagonist
Item
patients with a known allergy to any ace inhibitor or angiotensin receptor blocker
boolean
C0571939 (UMLS CUI [1])
C2585204 (UMLS CUI [2])
High risk Patients | Heart failure | Coronary Artery Disease Symptomatic | Hepatic impairment | Cerebrovascular accident | Myocardial Infarction
Item
high-risk patients [e.g. heart failure, symptomatic coronary artery disease, liver impairment, history of stroke or myocardial infarction]
boolean
C4319571 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
C0018801 (UMLS CUI [2])
C1956346 (UMLS CUI [3,1])
C0231220 (UMLS CUI [3,2])
C0948807 (UMLS CUI [4])
C0038454 (UMLS CUI [5])
C0027051 (UMLS CUI [6])
Hemoglobin measurement | Hematocrit measurement
Item
patients with hemoglobin < 10.5 [or hematocrit < 32]
boolean
C0518015 (UMLS CUI [1])
C0018935 (UMLS CUI [2])
Informed Consent Unable | Informed Consent Withdrawn
Item
inability to give, or withdraw, informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C2349954 (UMLS CUI [2,2])
Factor Preventing Completion of clinical trial | Clinical Test Result Abnormal | Mental Tests Abnormal | Laboratory test result abnormal
Item
other factors which in the investigator's opinion would prevent the patient from completing the protocol including clinically significant abnormalities in clinical, mental or laboratory testing
boolean
C1521761 (UMLS CUI [1,1])
C1292733 (UMLS CUI [1,2])
C2732579 (UMLS CUI [1,3])
C0456984 (UMLS CUI [2,1])
C0205161 (UMLS CUI [2,2])
C0025365 (UMLS CUI [3,1])
C0205161 (UMLS CUI [3,2])
C0438215 (UMLS CUI [4])
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