ID

33831

Beschrijving

Renal Denervation in Treatment Resistant Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01687725

Link

https://clinicaltrials.gov/show/NCT01687725

Trefwoorden

  1. 02-01-19 02-01-19 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

2 januari 2019

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Hypertension NCT01687725

Eligibility Hypertension NCT01687725

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
treatment resistant hypertension
Beschrijving

Hypertensive disease Unresponsive to Treatment

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0205269
male of female aged over 18 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
written informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
agreement to attend all study visits as planned in the protocol
Beschrijving

Protocol Compliance

Datatype

boolean

Alias
UMLS CUI [1]
C0525058
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
chronic kidney disease 3 - 5
Beschrijving

Chronic kidney disease stage

Datatype

boolean

Alias
UMLS CUI [1]
C2074731
any contradictions for mri
Beschrijving

Medical contraindication MRI

Datatype

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
claustrophobia
Beschrijving

Claustrophobia

Datatype

boolean

Alias
UMLS CUI [1]
C0008909
strabismus
Beschrijving

Strabismus

Datatype

boolean

Alias
UMLS CUI [1]
C0038379
severe ocular diseases
Beschrijving

Disorder of eye Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C0015397
UMLS CUI [1,2]
C0205082
history of epilepsia
Beschrijving

Epilepsy

Datatype

boolean

Alias
UMLS CUI [1]
C0014544

Similar models

Eligibility Hypertension NCT01687725

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Hypertensive disease Unresponsive to Treatment
Item
treatment resistant hypertension
boolean
C0020538 (UMLS CUI [1,1])
C0205269 (UMLS CUI [1,2])
Age
Item
male of female aged over 18 years
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
written informed consent
boolean
C0021430 (UMLS CUI [1])
Protocol Compliance
Item
agreement to attend all study visits as planned in the protocol
boolean
C0525058 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Chronic kidney disease stage
Item
chronic kidney disease 3 - 5
boolean
C2074731 (UMLS CUI [1])
Medical contraindication MRI
Item
any contradictions for mri
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
Claustrophobia
Item
claustrophobia
boolean
C0008909 (UMLS CUI [1])
Strabismus
Item
strabismus
boolean
C0038379 (UMLS CUI [1])
Disorder of eye Severe
Item
severe ocular diseases
boolean
C0015397 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Epilepsy
Item
history of epilepsia
boolean
C0014544 (UMLS CUI [1])

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