Englisch

Eligibility Knee Osteoarthritis NCT02036866

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 19-65
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
grade i or ii knee osteoarthritis confirmed by radiographs or other imaging and at least one of the following:
Beschreibung

Knee Osteoarthritis Grade Radiography | Knee Osteoarthritis Grade Imaging

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0409959
UMLS CUI [1,2]
C0441800
UMLS CUI [1,3]
C0034571
UMLS CUI [2,1]
C0409959
UMLS CUI [2,2]
C0441800
UMLS CUI [2,3]
C0011923
age > 50 years old
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
morning stiffness < 30 minutes
Beschreibung

Morning stiffness Duration

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0457086
UMLS CUI [1,2]
C0449238
crepitus
Beschreibung

Crepitus

Datentyp

boolean

Alias
UMLS CUI [1]
C0277964
meet at least 3 of 6 diagnostic criteria for osteoarthritis:
Beschreibung

Diagnostic criteria Fulfill Osteoarthritis

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0679228
UMLS CUI [1,2]
C1550543
UMLS CUI [1,3]
C0029408
age > 50 years old
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
morning stiffness < 30 minutes
Beschreibung

Morning stiffness Duration

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0457086
UMLS CUI [1,2]
C0449238
crepitus
Beschreibung

Crepitus

Datentyp

boolean

Alias
UMLS CUI [1]
C0277964
bony tenderness
Beschreibung

Bone tenderness

Datentyp

boolean

Alias
UMLS CUI [1]
C0238807
bony enlargement
Beschreibung

Bony joint enlargement

Datentyp

boolean

Alias
UMLS CUI [1]
C0221610
no palpable warmth
Beschreibung

Warmth Palpable Lacking

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0392197
UMLS CUI [1,2]
C0522499
UMLS CUI [1,3]
C0332268
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
bmi > 30
Beschreibung

Body mass index

Datentyp

boolean

Alias
UMLS CUI [1]
C1305855
history of traumatic spine or lower extremity injury within the last 6 months
Beschreibung

Spinal Injury | Lower extremity Injury

Datentyp

boolean

Alias
UMLS CUI [1]
C0037937
UMLS CUI [2]
C0023220
previous adverse reaction to electrical stimulation (i.e. burns or hypersensitivity)
Beschreibung

Adverse reaction Electric stimulation | Burns | Hypersensitivity

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0559546
UMLS CUI [1,2]
C0013786
UMLS CUI [2]
C0006434
UMLS CUI [3]
C0020517
cardiac pacemaker
Beschreibung

Artificial cardiac pacemaker

Datentyp

boolean

Alias
UMLS CUI [1]
C0030163
metal implants in head
Beschreibung

Metallic implant Head

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3693688
UMLS CUI [1,2]
C0018670
current pregnancy
Beschreibung

Pregnancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
neurological disorders
Beschreibung

Nervous system disorder

Datentyp

boolean

Alias
UMLS CUI [1]
C0027765
history of seizures
Beschreibung

Seizures

Datentyp

boolean

Alias
UMLS CUI [1]
C0036572
unable to give consent or understand the procedures of this study
Beschreibung

Informed Consent Unable | Comprehension Study Protocol Unable

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0162340
UMLS CUI [2,2]
C2348563
UMLS CUI [2,3]
C1299582
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Ähnliche Modelle

Eligibility Knee Osteoarthritis NCT02036866

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age 19-65
boolean
C0001779 (UMLS CUI [1])
Knee Osteoarthritis Grade Radiography | Knee Osteoarthritis Grade Imaging
Item
grade i or ii knee osteoarthritis confirmed by radiographs or other imaging and at least one of the following:
boolean
C0409959 (UMLS CUI [1,1])
C0441800 (UMLS CUI [1,2])
C0034571 (UMLS CUI [1,3])
C0409959 (UMLS CUI [2,1])
C0441800 (UMLS CUI [2,2])
C0011923 (UMLS CUI [2,3])
Age
Item
age > 50 years old
boolean
C0001779 (UMLS CUI [1])
Morning stiffness Duration
Item
morning stiffness < 30 minutes
boolean
C0457086 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Crepitus
Item
crepitus
boolean
C0277964 (UMLS CUI [1])
Diagnostic criteria Fulfill Osteoarthritis
Item
meet at least 3 of 6 diagnostic criteria for osteoarthritis:
boolean
C0679228 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
C0029408 (UMLS CUI [1,3])
Age
Item
age > 50 years old
boolean
C0001779 (UMLS CUI [1])
Morning stiffness Duration
Item
morning stiffness < 30 minutes
boolean
C0457086 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Crepitus
Item
crepitus
boolean
C0277964 (UMLS CUI [1])
Bone tenderness
Item
bony tenderness
boolean
C0238807 (UMLS CUI [1])
Bony joint enlargement
Item
bony enlargement
boolean
C0221610 (UMLS CUI [1])
Warmth Palpable Lacking
Item
no palpable warmth
boolean
C0392197 (UMLS CUI [1,1])
C0522499 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Body mass index
Item
bmi > 30
boolean
C1305855 (UMLS CUI [1])
Spinal Injury | Lower extremity Injury
Item
history of traumatic spine or lower extremity injury within the last 6 months
boolean
C0037937 (UMLS CUI [1])
C0023220 (UMLS CUI [2])
Adverse reaction Electric stimulation | Burns | Hypersensitivity
Item
previous adverse reaction to electrical stimulation (i.e. burns or hypersensitivity)
boolean
C0559546 (UMLS CUI [1,1])
C0013786 (UMLS CUI [1,2])
C0006434 (UMLS CUI [2])
C0020517 (UMLS CUI [3])
Artificial cardiac pacemaker
Item
cardiac pacemaker
boolean
C0030163 (UMLS CUI [1])
Metallic implant Head
Item
metal implants in head
boolean
C3693688 (UMLS CUI [1,1])
C0018670 (UMLS CUI [1,2])
Pregnancy
Item
current pregnancy
boolean
C0032961 (UMLS CUI [1])
Nervous system disorder
Item
neurological disorders
boolean
C0027765 (UMLS CUI [1])
Seizures
Item
history of seizures
boolean
C0036572 (UMLS CUI [1])
Informed Consent Unable | Comprehension Study Protocol Unable
Item
unable to give consent or understand the procedures of this study
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0162340 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
C1299582 (UMLS CUI [2,3])
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