ID

13125

Beschrijving

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

Link

https://clinicaltrials.gov/show/NCT00122811

Trefwoorden

  1. 18-01-16 18-01-16 -
Geüploaded op

18 januari 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Hypertension NCT00122811

Eligibility Hypertension NCT00122811

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 80 or older
Beschrijving

age

Datatype

boolean

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

bp

Datatype

boolean

Alias
UMLS CUI [1]
C0005823
Exclusion Criteria
Beschrijving

Exclusion Criteria

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

accelerated hypertension

Datatype

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.
Beschrijving

congestive heart failure, ace inhibitor, digoxin

Datatype

boolean

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

creatinine

Datatype

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.)
Beschrijving

subarachnoid haemorrhage

Datatype

boolean

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

comorbidity

Datatype

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).
Beschrijving

secondary hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C0155616
gout.
Beschrijving

gout

Datatype

boolean

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

dementia

Datatype

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).
Beschrijving

nursing home

Datatype

boolean

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

walking

Datatype

boolean

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

study subject participation status

Datatype

boolean

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

substance abuse

Datatype

boolean

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

placebo

Datatype

boolean

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

contraindication

Datatype

boolean

Alias
UMLS CUI [1]
C1301624

Similar models

Eligibility Hypertension NCT00122811

Name
Type
Description | Question | Decode (Coded Value)
Datatype
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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