Informações:
Falhas:
ID
40037
Descrição
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
Palavras-chave
Versões (1)
- 10/03/2020 10/03/2020 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
10 de março de 2020
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Hypertension NCT01525108
Eligibility Hypertension NCT01525108
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT01525108
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Outpatients | Age
Item
ambulatory patients older than 18
boolean
C0029921 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
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])
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])
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])
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])
C1524063 (UMLS CUI [1,2])
C0727798 (UMLS CUI [1,3])
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])
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])
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])
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])
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])
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])
C0013956 (UMLS CUI [1,2])
C4288399 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])