ID

36550

Description

Decompressive Cervical Surgery and Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT02016768

Link

https://clinicaltrials.gov/show/NCT02016768

Keywords

  1. 5/21/19 5/21/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

May 21, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Myelopathy, Compressive NCT02016768

Eligibility Myelopathy, Compressive NCT02016768

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
established diagnosis of cervical spondylosis myelopathy
Description

Cervical spondylosis with myelopathy

Data type

boolean

Alias
UMLS CUI [1]
C0158242
be at least 18 years of age
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
office-measured systolic bp≧140mmhg
Description

Systolic Pressure

Data type

boolean

Alias
UMLS CUI [1]
C0871470
ability to adhere to study protocol
Description

Protocol Compliance

Data type

boolean

Alias
UMLS CUI [1]
C0525058
have signed an approved informed consent form for participation in this study
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
have hypertension secondary to a treatable cause
Description

Hypertensive disease Secondary to Cause | Cause Reversible

Data type

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0175668
UMLS CUI [1,3]
C0015127
UMLS CUI [2,1]
C0015127
UMLS CUI [2,2]
C0205343
have prior cervical spine surgery
Description

Cervical spine surgery

Data type

boolean

Alias
UMLS CUI [1]
C0742216
are pregnant or contemplating pregnancy during the 3-month follow-up period
Description

Pregnancy | Pregnancy, Planned

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
people deny to join the study
Description

Study Subject Participation Status Denial

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C2700401
are unable to comply with protocol requirements
Description

Protocol Compliance Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C1299582
are unlikely to survive the protocol follow-up period
Description

Life Expectancy Limited | Survival Follow-up Unlikely

Data type

boolean

Alias
UMLS CUI [1,1]
C0023671
UMLS CUI [1,2]
C0439801
UMLS CUI [2,1]
C0038952
UMLS CUI [2,2]
C3274571
UMLS CUI [2,3]
C0750558
are enrolled in another concurrent clinical trial
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
visual analogue scale≥4
Description

Visual Analog Scale

Data type

boolean

Alias
UMLS CUI [1]
C3536884

Similar models

Eligibility Myelopathy, Compressive NCT02016768

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Cervical spondylosis with myelopathy
Item
established diagnosis of cervical spondylosis myelopathy
boolean
C0158242 (UMLS CUI [1])
Age
Item
be at least 18 years of age
boolean
C0001779 (UMLS CUI [1])
Systolic Pressure
Item
office-measured systolic bp≧140mmhg
boolean
C0871470 (UMLS CUI [1])
Protocol Compliance
Item
ability to adhere to study protocol
boolean
C0525058 (UMLS CUI [1])
Informed Consent
Item
have signed an approved informed consent form for participation in this study
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Hypertensive disease Secondary to Cause | Cause Reversible
Item
have hypertension secondary to a treatable cause
boolean
C0020538 (UMLS CUI [1,1])
C0175668 (UMLS CUI [1,2])
C0015127 (UMLS CUI [1,3])
C0015127 (UMLS CUI [2,1])
C0205343 (UMLS CUI [2,2])
Cervical spine surgery
Item
have prior cervical spine surgery
boolean
C0742216 (UMLS CUI [1])
Pregnancy | Pregnancy, Planned
Item
are pregnant or contemplating pregnancy during the 3-month follow-up period
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Study Subject Participation Status Denial
Item
people deny to join the study
boolean
C2348568 (UMLS CUI [1,1])
C2700401 (UMLS CUI [1,2])
Protocol Compliance Unable
Item
are unable to comply with protocol requirements
boolean
C0525058 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Life Expectancy Limited | Survival Follow-up Unlikely
Item
are unlikely to survive the protocol follow-up period
boolean
C0023671 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0038952 (UMLS CUI [2,1])
C3274571 (UMLS CUI [2,2])
C0750558 (UMLS CUI [2,3])
Study Subject Participation Status
Item
are enrolled in another concurrent clinical trial
boolean
C2348568 (UMLS CUI [1])
Visual Analog Scale
Item
visual analogue scale≥4
boolean
C3536884 (UMLS CUI [1])

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