Informatie:
Fout:
ID
29992
Beschrijving
Surveillance of Efficacy and Safety of Drug PRITOR in patieNts With Arterial Hypertension, Who do Not Tolerate ACE inhibitoR Treatment; ODM derived from: https://clinicaltrials.gov/show/NCT00932867
Link
https://clinicaltrials.gov/show/NCT00932867
Trefwoorden
Versies (1)
- 03-05-18 03-05-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
3 mei 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Hypertension NCT00932867
Eligibility Hypertension NCT00932867
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT00932867
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
patients over 18 years of age
boolean
C0001779 (UMLS CUI [1])
Hypertensive disease | Systolic Pressure | Diastolic blood pressure
Item
arterial hypertension (sbp < 160 mmhg and dbp < 100 mmhg)
boolean
C0020538 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Intolerance to Angiotensin-Converting Enzyme Inhibitors
Item
patients, who do not tolerate ace inhibitors (must be documented in the official ambulant documentation)
boolean
C1744706 (UMLS CUI [1,1])
C0003015 (UMLS CUI [1,2])
C0003015 (UMLS CUI [1,2])
Inclusion criteria Control Arm | Angiotensin-Converting Enzyme Inhibitors
Item
inclusion criteria for the control arm (treated by acei):
boolean
C1512693 (UMLS CUI [1,1])
C0009932 (UMLS CUI [1,2])
C1522541 (UMLS CUI [1,3])
C0003015 (UMLS CUI [2])
C0009932 (UMLS CUI [1,2])
C1522541 (UMLS CUI [1,3])
C0003015 (UMLS CUI [2])
Age
Item
patients over 18 years of age
boolean
C0001779 (UMLS CUI [1])
Hypertensive disease | Systolic Pressure | Diastolic blood pressure
Item
arterial hypertension (sbp < 160 mmhg and dbp < 100 mmhg)
boolean
C0020538 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Angiotensin-Converting Enzyme Inhibitors Receive Ability
Item
patients, who tolerate acei treatment
boolean
C0003015 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
C1514756 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
Cholestasis | Hepatic Insufficiency Severe
Item
cholestasis, severe hepatic insufficiency
boolean
C0008370 (UMLS CUI [1])
C1306571 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C1306571 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Hypersensitivity Telmisartan
Item
allergy to telmisartan
boolean
C0020517 (UMLS CUI [1,1])
C0248719 (UMLS CUI [1,2])
C0248719 (UMLS CUI [1,2])
Gravidity | Breast Feeding
Item
gravidity or lactation
boolean
C0600457 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Exclusion Criteria Control Arm | Angiotensin-Converting Enzyme Inhibitors
Item
exclusion criteria for the arm of patient treated by acei:
boolean
C0680251 (UMLS CUI [1,1])
C0009932 (UMLS CUI [1,2])
C1522541 (UMLS CUI [1,3])
C0003015 (UMLS CUI [2])
C0009932 (UMLS CUI [1,2])
C1522541 (UMLS CUI [1,3])
C0003015 (UMLS CUI [2])
Cholestasis | Hepatic Insufficiency Severe
Item
cholestasis, severe hepatic insufficiency
boolean
C0008370 (UMLS CUI [1])
C1306571 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C1306571 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Angiotensin-converting-enzyme inhibitor allergy
Item
allergy to acei
boolean
C0571939 (UMLS CUI [1])
Gravidity | Breast Feeding
Item
gravidity or lactation
boolean
C0600457 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])