ID

39978

Beschreibung

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

Link

https://clinicaltrials.gov/show/NCT01292694

Stichworte

Versionen (1)
  1. 07.03.20 07.03.20 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

7. März 2020

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Hypertension NCT01292694

Englisch

Eligibility Hypertension NCT01292694

1 Formulare  
Inclusion Criteria
Beschreibung

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]
Beschreibung

Autonomic Failure | Supine hypertension | Participation Clinical Trial Specified

Datentyp

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
Beschreibung

Supine hypertension | Systolic Pressure | Diastolic blood pressure

Datentyp

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
Beschreibung

Racial group All | Age

Datentyp

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
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
all medical students
Beschreibung

Medical Students All

Datentyp

boolean

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

Pregnancy

Datentyp

boolean

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

Angioedema

Datentyp

boolean

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

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

Datentyp

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]
Beschreibung

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

Datentyp

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]
Beschreibung

Hemoglobin measurement | Hematocrit measurement

Datentyp

boolean

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

Informed Consent Unable | Informed Consent Withdrawn

Datentyp

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
Beschreibung

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

Datentyp

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
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Hypertension NCT01292694

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])
Zum Seitenanfang zurückkehren 

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