ID

40037

Beschrijving

A Home-based Blood Pressure Monitoring Program to Promote Better Management of Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01525108

Link

https://clinicaltrials.gov/show/NCT01525108

Trefwoorden

Versies (1)
  1. 10-03-20 10-03-20 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

10 maart 2020

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Hypertension NCT01525108

Engels

Eligibility Hypertension NCT01525108

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
ambulatory patients older than 18
Beschrijving

Outpatients | Age

Datatype

boolean

Alias
UMLS CUI [1]
C0029921
UMLS CUI [2]
C0001779
patients newly diagnosed as hypertension stage 1
Beschrijving

Hypertensive disease Newly Diagnosed Stage

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C1518321
UMLS CUI [1,3]
C0699749
patients previously on antihypertensive treatment but uncontrolled hypertension
Beschrijving

Antihypertensive therapy Previous | Uncontrolled hypertension

Datatype

boolean

Alias
UMLS CUI [1,1]
C0585941
UMLS CUI [1,2]
C0205156
UMLS CUI [2]
C1868885
patients not possessing electronic self blood pressure measurement device
Beschrijving

Self Taking Manual Blood Pressure Unavailable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0727798
UMLS CUI [1,2]
C0686905
patients with functional ability to use the device
Beschrijving

Ability Use of Self Taking Manual Blood Pressure

Datatype

boolean

Alias
UMLS CUI [1,1]
C0085732
UMLS CUI [1,2]
C1524063
UMLS CUI [1,3]
C0727798
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients requiring two or more antihypertensive drugs at the start of the study
Beschrijving

Antihypertensive Agents Quantity Required

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003364
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C1514873
patients with secondary hypertension
Beschrijving

Secondary hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C0155616
patients cardiovascular comorbidities and other interfering medical conditions
Beschrijving

Comorbidity Cardiovascular | Other medical condition Interfering

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C3887460
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C0521102
patients with drug contraindication or documented drug allergy
Beschrijving

Medical contraindication Drugs | Drug Allergy

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0013227
UMLS CUI [2]
C0013182
patients with serum creatinine > 150 microliters
Beschrijving

Creatinine measurement, serum

Datatype

boolean

Alias
UMLS CUI [1]
C0201976
withdrawal criteria:
Beschrijving

Withdrawal criteria

Datatype

boolean

Alias
UMLS CUI [1,1]
C2349954
UMLS CUI [1,2]
C0243161
inadequate therapeutic effect requiring an increase of more than 20% in pre-established number of visits
Beschrijving

Therapeutic Effect Inadequate

Datatype

boolean

Alias
UMLS CUI [1,1]
C1527144
UMLS CUI [1,2]
C0205412
emergence of adverse drug reactions requiring cessation of medication
Beschrijving

Adverse reaction to drug Emergency Situation | Pharmacotherapy Discontinuation Required

Datatype

boolean

Alias
UMLS CUI [1,1]
C0041755
UMLS CUI [1,2]
C0013956
UMLS CUI [2,1]
C4288399
UMLS CUI [2,2]
C1514873
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Similar models

Eligibility Hypertension NCT01525108

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Outpatients | Age
Item
ambulatory patients older than 18
boolean
C0029921 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Hypertensive disease Newly Diagnosed Stage
Item
patients newly diagnosed as hypertension stage 1
boolean
C0020538 (UMLS CUI [1,1])
C1518321 (UMLS CUI [1,2])
C0699749 (UMLS CUI [1,3])
Antihypertensive therapy Previous | Uncontrolled hypertension
Item
patients previously on antihypertensive treatment but uncontrolled hypertension
boolean
C0585941 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C1868885 (UMLS CUI [2])
Self Taking Manual Blood Pressure Unavailable
Item
patients not possessing electronic self blood pressure measurement device
boolean
C0727798 (UMLS CUI [1,1])
C0686905 (UMLS CUI [1,2])
Ability Use of Self Taking Manual Blood Pressure
Item
patients with functional ability to use the device
boolean
C0085732 (UMLS CUI [1,1])
C1524063 (UMLS CUI [1,2])
C0727798 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Antihypertensive Agents Quantity Required
Item
patients requiring two or more antihypertensive drugs at the start of the study
boolean
C0003364 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1514873 (UMLS CUI [1,3])
Secondary hypertension
Item
patients with secondary hypertension
boolean
C0155616 (UMLS CUI [1])
Comorbidity Cardiovascular | Other medical condition Interfering
Item
patients cardiovascular comorbidities and other interfering medical conditions
boolean
C0009488 (UMLS CUI [1,1])
C3887460 (UMLS CUI [1,2])
C3843040 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
Medical contraindication Drugs | Drug Allergy
Item
patients with drug contraindication or documented drug allergy
boolean
C1301624 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0013182 (UMLS CUI [2])
Creatinine measurement, serum
Item
patients with serum creatinine > 150 microliters
boolean
C0201976 (UMLS CUI [1])
Withdrawal criteria
Item
withdrawal criteria:
boolean
C2349954 (UMLS CUI [1,1])
C0243161 (UMLS CUI [1,2])
Therapeutic Effect Inadequate
Item
inadequate therapeutic effect requiring an increase of more than 20% in pre-established number of visits
boolean
C1527144 (UMLS CUI [1,1])
C0205412 (UMLS CUI [1,2])
Adverse reaction to drug Emergency Situation | Pharmacotherapy Discontinuation Required
Item
emergence of adverse drug reactions requiring cessation of medication
boolean
C0041755 (UMLS CUI [1,1])
C0013956 (UMLS CUI [1,2])
C4288399 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
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