ID

13125

Beskrivning

The Hypertension in the Very Elderly Trial (HYVET); ODM derived from: https://clinicaltrials.gov/show/NCT00122811

Länk

https://clinicaltrials.gov/show/NCT00122811

Nyckelord

  1. 2016-01-18 2016-01-18 -
Uppladdad den

18 januari 2016

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Hypertension NCT00122811

Eligibility Hypertension NCT00122811

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 80 or older
Beskrivning

age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
sitting systolic bp 160-199 mmhg and sitting diastolic bp < 110 mmhg
Beskrivning

bp

Datatyp

boolean

Alias
UMLS CUI [1]
C0005823
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
known accelerated hypertension (retinal haemorrhages or exudates or papilloedema).
Beskrivning

accelerated hypertension

Datatyp

boolean

Alias
UMLS CUI [1]
C0020540
overt clinical congestive heart failure requiring treatment with a diuretic or angiotensin converting enzyme inhibitor. subjects allowed if treated with digoxin only.
Beskrivning

congestive heart failure, ace inhibitor, digoxin

Datatyp

boolean

Alias
UMLS CUI [1]
C0018802
UMLS CUI [2]
C0003015
UMLS CUI [3]
C0012265
renal failure (serum creatinine of more than 150 µmol/l).
Beskrivning

creatinine

Datatyp

boolean

Alias
UMLS CUI [1]
C0201976
previous documented cerebral or subarachnoid haemorrhage in the last 6 months. (ischaemic cerebral and cardiac events do not exclude, although the patient must be neurologically and cardiologically stable.)
Beskrivning

subarachnoid haemorrhage

Datatyp

boolean

Alias
UMLS CUI [1]
C0038525
UMLS CUI [2]
C2937358
condition expected to severely limit survival, e.g. terminal illness.
Beskrivning

comorbidity

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205082
known secondary hypertension (e.g. renal artery stenosis, chronic renal insufficiency, and endocrine cause).
Beskrivning

secondary hypertension

Datatyp

boolean

Alias
UMLS CUI [1]
C0155616
gout.
Beskrivning

gout

Datatyp

boolean

Alias
UMLS CUI [1]
C0018099
clinical diagnosis of dementia.
Beskrivning

dementia

Datatyp

boolean

Alias
UMLS CUI [1]
C0497327
resident in a nursing home, i.e. where the dependency and care requirements of the patients are such that they require the regular input of qualified nurses and therefore the majority of staff in the home are nurses (other forms of residential care are acceptable).
Beskrivning

nursing home

Datatyp

boolean

Alias
UMLS CUI [1]
C0028688
unable to stand up or walk
Beskrivning

walking

Datatyp

boolean

Alias
UMLS CUI [1]
C0080331
participation in a drug trial within the past month preceding selection.
Beskrivning

study subject participation status

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
alcohol or drug abuse.
Beskrivning

substance abuse

Datatyp

boolean

Alias
UMLS CUI [1]
C0038586
less than 2 months placebo run-in.
Beskrivning

placebo

Datatyp

boolean

Alias
UMLS CUI [1]
C0032042
contraindications to use of trial drugs
Beskrivning

contraindication

Datatyp

boolean

Alias
UMLS CUI [1]
C1301624

Similar models

Eligibility Hypertension NCT00122811

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
aged 80 or older
boolean
C0001779 (UMLS CUI [1])
bp
Item
sitting systolic bp 160-199 mmhg and sitting diastolic bp < 110 mmhg
boolean
C0005823 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
accelerated hypertension
Item
known accelerated hypertension (retinal haemorrhages or exudates or papilloedema).
boolean
C0020540 (UMLS CUI [1])
congestive heart failure, ace inhibitor, digoxin
Item
overt clinical congestive heart failure requiring treatment with a diuretic or angiotensin converting enzyme inhibitor. subjects allowed if treated with digoxin only.
boolean
C0018802 (UMLS CUI [1])
C0003015 (UMLS CUI [2])
C0012265 (UMLS CUI [3])
creatinine
Item
renal failure (serum creatinine of more than 150 µmol/l).
boolean
C0201976 (UMLS CUI [1])
subarachnoid haemorrhage
Item
previous documented cerebral or subarachnoid haemorrhage in the last 6 months. (ischaemic cerebral and cardiac events do not exclude, although the patient must be neurologically and cardiologically stable.)
boolean
C0038525 (UMLS CUI [1])
C2937358 (UMLS CUI [2])
comorbidity
Item
condition expected to severely limit survival, e.g. terminal illness.
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
secondary hypertension
Item
known secondary hypertension (e.g. renal artery stenosis, chronic renal insufficiency, and endocrine cause).
boolean
C0155616 (UMLS CUI [1])
gout
Item
gout.
boolean
C0018099 (UMLS CUI [1])
dementia
Item
clinical diagnosis of dementia.
boolean
C0497327 (UMLS CUI [1])
nursing home
Item
resident in a nursing home, i.e. where the dependency and care requirements of the patients are such that they require the regular input of qualified nurses and therefore the majority of staff in the home are nurses (other forms of residential care are acceptable).
boolean
C0028688 (UMLS CUI [1])
walking
Item
unable to stand up or walk
boolean
C0080331 (UMLS CUI [1])
study subject participation status
Item
participation in a drug trial within the past month preceding selection.
boolean
C2348568 (UMLS CUI [1])
substance abuse
Item
alcohol or drug abuse.
boolean
C0038586 (UMLS CUI [1])
placebo
Item
less than 2 months placebo run-in.
boolean
C0032042 (UMLS CUI [1])
contraindication
Item
contraindications to use of trial drugs
boolean
C1301624 (UMLS CUI [1])

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