Informatie:
Fout:
ID
40323
Beschrijving
Efficiency of Monitoring and Control Program of Hypertension Through Pharmacy Offices. APOF Project; ODM derived from: https://clinicaltrials.gov/show/NCT02032472
Link
https://clinicaltrials.gov/show/NCT02032472
Trefwoorden
Versies (1)
- 08-04-20 08-04-20 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
8 april 2020
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility Hypertension NCT02032472
Eligibility Hypertension NCT02032472
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT02032472
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
age not less than 18 years
boolean
C0001779 (UMLS CUI [1])
Hypertensive disease Controlled Duration
Item
hta controlled over 2 years of evolution
boolean
C0020538 (UMLS CUI [1,1])
C2911690 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
C2911690 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Medical History Participation Health center | Residence Stable Geographic area
Item
subjects with a history open to participating health centers or stable residence in the geographic area
boolean
C0262926 (UMLS CUI [1,1])
C0679823 (UMLS CUI [1,2])
C0475309 (UMLS CUI [1,3])
C0237096 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
C0017446 (UMLS CUI [2,3])
C0679823 (UMLS CUI [1,2])
C0475309 (UMLS CUI [1,3])
C0237096 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
C0017446 (UMLS CUI [2,3])
Study Subject Participation Status Agreement
Item
subjects who agree to participate
boolean
C2348568 (UMLS CUI [1,1])
C0680240 (UMLS CUI [1,2])
C0680240 (UMLS CUI [1,2])
Comorbidity | Diabetes Mellitus | Heart failure | Kidney Failure
Item
comorbidity and concomitant (diabetes mellitus, heart failure or renal failure
boolean
C0009488 (UMLS CUI [1])
C0011849 (UMLS CUI [2])
C0018801 (UMLS CUI [3])
C0035078 (UMLS CUI [4])
C0011849 (UMLS CUI [2])
C0018801 (UMLS CUI [3])
C0035078 (UMLS CUI [4])
Residence Temporary | Geographic area Clinical Trial
Item
patients with temporary residence in the geographic area of study
boolean
C0237096 (UMLS CUI [1,1])
C0205374 (UMLS CUI [1,2])
C0017446 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C0205374 (UMLS CUI [1,2])
C0017446 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
Hypertensive disease Controlled by Health Professionals
Item
subjects of hypertension controlled by outside professionals to our primary care teams.
boolean
C0020538 (UMLS CUI [1,1])
C0332298 (UMLS CUI [1,2])
C1704312 (UMLS CUI [1,3])
C0332298 (UMLS CUI [1,2])
C1704312 (UMLS CUI [1,3])
Home care of patient | Patient Transfer Clinic Unsuccessful
Item
subjects with home care or any other cause which does not permit their displacement, transfer to the clinic or pharmacy during the evaluation period.
boolean
C0204977 (UMLS CUI [1])
C0030704 (UMLS CUI [2,1])
C0442592 (UMLS CUI [2,2])
C1272705 (UMLS CUI [2,3])
C0030704 (UMLS CUI [2,1])
C0442592 (UMLS CUI [2,2])
C1272705 (UMLS CUI [2,3])
Disease Severe | Prognosis bad | Life Expectancy
Item
subjects with severe diseases of poor prognosis, hopefully less than one year of life.
boolean
C0012634 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0278252 (UMLS CUI [2])
C0023671 (UMLS CUI [3])
C0205082 (UMLS CUI [1,2])
C0278252 (UMLS CUI [2])
C0023671 (UMLS CUI [3])
Telephone Lacking
Item
subjects who do not have telephones.
boolean
C0039457 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,2])
Communication impairment | Impaired cognition | Hypesthesia | Language Barriers
Item
subjects with communication problems (cognitive impairment, sensory, language barrier)
boolean
C0009460 (UMLS CUI [1])
C0338656 (UMLS CUI [2])
C0020580 (UMLS CUI [3])
C0237167 (UMLS CUI [4])
C0338656 (UMLS CUI [2])
C0020580 (UMLS CUI [3])
C0237167 (UMLS CUI [4])