ID

17656

Beschreibung

Ambulatory Blood Pressure Monitoring in Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT00166634

Link

https://clinicaltrials.gov/show/NCT00166634

Stichworte

Versionen (2)
  1. 27.09.16 27.09.16 -
  2. 20.09.21 20.09.21 -
Hochgeladen am

27. September 2016

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility Hypertension NCT00166634

Englisch

Eligibility Hypertension NCT00166634

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and female children 5-16 years of age.
Beschreibung

Child | Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0008059
UMLS CUI [2]
C0001779
borderline or mild systolic and or diastolic hypertension as defined by 1996 task force criteria.
Beschreibung

Borderline hypertension | Systolic hypertension, mild | Diastolic hypertension

Datentyp

boolean

Alias
UMLS CUI [1]
C0262395
UMLS CUI [2]
C1845210
UMLS CUI [3]
C0235222
no current drug therapy for hypertension being taken.
Beschreibung

Pharmacotherapy Hypertensive disease

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0020538
must be ambulatory and willing to wear an abp monitor for 24 hours
Beschreibung

Outpatient | 24-hour ambulatory blood pressure monitoring Willing

Datentyp

boolean

Alias
UMLS CUI [1]
C0029921
UMLS CUI [2,1]
C2022220
UMLS CUI [2,2]
C0600109
agree to refrain from swimming, showering and other activities that might result in damage to abp monitor during the two 24 hour intervals that the monitor is worn.
Beschreibung

Swimming omit | showering omit | Physical activity omit Preventing 24-hour ambulatory blood pressure monitoring

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0039003
UMLS CUI [1,2]
C0750563
UMLS CUI [2,1]
C2322572
UMLS CUI [2,2]
C0750563
UMLS CUI [3,1]
C0026606
UMLS CUI [3,2]
C0750563
UMLS CUI [3,3]
C1292733
UMLS CUI [3,4]
C2022220
standing height between 45 inches and 73 inches
Beschreibung

Standing height

Datentyp

boolean

Alias
UMLS CUI [1]
C0424645
informed parental consent and patient assent.
Beschreibung

Informed Consent parent | Assent Patient

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0030551
UMLS CUI [2,1]
C1879749
UMLS CUI [2,2]
C0030705
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe or life threatening hypertension.
Beschreibung

Hypertension, severe | Hypertensive disease Life Threatening

Datentyp

boolean

Alias
UMLS CUI [1]
C4013784
UMLS CUI [2,1]
C0020538
UMLS CUI [2,2]
C2826244
any drug therapy that may raise or lower the blood pressure.
Beschreibung

Pharmacotherapy Causing Increase in blood pressure | Pharmacotherapy Causing Decreased Blood Pressure

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0678227
UMLS CUI [1,3]
C0497247
UMLS CUI [2,1]
C0013216
UMLS CUI [2,2]
C0678227
UMLS CUI [2,3]
C2917141
any severe bleeding disorder or concurrent treatment with anticoagulant medications
Beschreibung

Blood Coagulation Disorder Severe | Anticoagulants

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0005779
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C0003280
non-ambulatory
Beschreibung

Outpatient

Datentyp

boolean

Alias
UMLS CUI [1]
C0029921
significant arrhythmia
Beschreibung

Cardiac Arrhythmia Significant

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0003811
UMLS CUI [1,2]
C0750502
previous history of significant non-compliance with prescribed medical care.
Beschreibung

Compliance behavior Limited Significant

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0750502
any other disease that, in the opinion of the investigator, might interfere with the accurate measurement of the blood pressure or place the subject at risk unnecessarily.
Beschreibung

Disease Interferes with Blood pressure measurement | Disease Study Subject At risk

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C3826646
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C0681850
UMLS CUI [2,3]
C1444641
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Ähnliche Modelle

Eligibility Hypertension NCT00166634

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Child | Age
Item
male and female children 5-16 years of age.
boolean
C0008059 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Borderline hypertension | Systolic hypertension, mild | Diastolic hypertension
Item
borderline or mild systolic and or diastolic hypertension as defined by 1996 task force criteria.
boolean
C0262395 (UMLS CUI [1])
C1845210 (UMLS CUI [2])
C0235222 (UMLS CUI [3])
Pharmacotherapy Hypertensive disease
Item
no current drug therapy for hypertension being taken.
boolean
C0013216 (UMLS CUI [1,1])
C0020538 (UMLS CUI [1,2])
Outpatient | 24-hour ambulatory blood pressure monitoring Willing
Item
must be ambulatory and willing to wear an abp monitor for 24 hours
boolean
C0029921 (UMLS CUI [1])
C2022220 (UMLS CUI [2,1])
C0600109 (UMLS CUI [2,2])
Swimming omit | showering omit | Physical activity omit Preventing 24-hour ambulatory blood pressure monitoring
Item
agree to refrain from swimming, showering and other activities that might result in damage to abp monitor during the two 24 hour intervals that the monitor is worn.
boolean
C0039003 (UMLS CUI [1,1])
C0750563 (UMLS CUI [1,2])
C2322572 (UMLS CUI [2,1])
C0750563 (UMLS CUI [2,2])
C0026606 (UMLS CUI [3,1])
C0750563 (UMLS CUI [3,2])
C1292733 (UMLS CUI [3,3])
C2022220 (UMLS CUI [3,4])
Standing height
Item
standing height between 45 inches and 73 inches
boolean
C0424645 (UMLS CUI [1])
Informed Consent parent | Assent Patient
Item
informed parental consent and patient assent.
boolean
C0021430 (UMLS CUI [1,1])
C0030551 (UMLS CUI [1,2])
C1879749 (UMLS CUI [2,1])
C0030705 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Hypertension, severe | Hypertensive disease Life Threatening
Item
severe or life threatening hypertension.
boolean
C4013784 (UMLS CUI [1])
C0020538 (UMLS CUI [2,1])
C2826244 (UMLS CUI [2,2])
Pharmacotherapy Causing Increase in blood pressure | Pharmacotherapy Causing Decreased Blood Pressure
Item
any drug therapy that may raise or lower the blood pressure.
boolean
C0013216 (UMLS CUI [1,1])
C0678227 (UMLS CUI [1,2])
C0497247 (UMLS CUI [1,3])
C0013216 (UMLS CUI [2,1])
C0678227 (UMLS CUI [2,2])
C2917141 (UMLS CUI [2,3])
Blood Coagulation Disorder Severe | Anticoagulants
Item
any severe bleeding disorder or concurrent treatment with anticoagulant medications
boolean
C0005779 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0003280 (UMLS CUI [2])
Outpatient
Item
non-ambulatory
boolean
C0029921 (UMLS CUI [1])
Cardiac Arrhythmia Significant
Item
significant arrhythmia
boolean
C0003811 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
Compliance behavior Limited Significant
Item
previous history of significant non-compliance with prescribed medical care.
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0750502 (UMLS CUI [1,3])
Disease Interferes with Blood pressure measurement | Disease Study Subject At risk
Item
any other disease that, in the opinion of the investigator, might interfere with the accurate measurement of the blood pressure or place the subject at risk unnecessarily.
boolean
C0012634 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C3826646 (UMLS CUI [1,3])
C0012634 (UMLS CUI [2,1])
C0681850 (UMLS CUI [2,2])
C1444641 (UMLS CUI [2,3])
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