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])