Eligibility Osteoarthritis, Knee NCT00820430

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
participants must be >18 years old;
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
participants must have a kl score between 0 and 3;
Description

kl score

Type de données

boolean

Alias
UMLS CUI [1]
C3177117
participants must have clearance to use protocol specified equipment: 3t mri with parallel imaging capability and phased array knee coil (minimum 4 elements);
Description

protocol specified equipment, 3t mri

Type de données

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0014672
UMLS CUI [1,3]
C2985394
participant had no change of treatment occur within the last 6 months;
Description

treatment change

Type de données

boolean

Alias
UMLS CUI [1]
C1299575
participants have no plans of changing to a different treatment within the next 3 months;
Description

treatment change

Type de données

boolean

Alias
UMLS CUI [1]
C1299575
participant must provide a study-specific signed informed consent form.
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with contraindication to 3t mri: claustrophobia, implanted metal or medical device that is not approved for mri scanning at 3t, pregnancy, inability to tolerate relative immobility for 1 hour;
Description

3t mri contraindication

Type de données

boolean

Alias
UMLS CUI [1,1]
C2985394
UMLS CUI [1,2]
C1301624
patients with prior knee surgery or trauma of the knee;
Description

knee surgery, knee trauma

Type de données

boolean

Alias
UMLS CUI [1]
C0187769
UMLS CUI [2]
C0022744
patients with kl score of 4.
Description

kl score

Type de données

boolean

Alias
UMLS CUI [1]
C3177117

Similar models

Eligibility Osteoarthritis, Knee NCT00820430

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
participants must be >18 years old;
boolean
C0001779 (UMLS CUI [1])
kl score
Item
participants must have a kl score between 0 and 3;
boolean
C3177117 (UMLS CUI [1])
protocol specified equipment, 3t mri
Item
participants must have clearance to use protocol specified equipment: 3t mri with parallel imaging capability and phased array knee coil (minimum 4 elements);
boolean
C2348563 (UMLS CUI [1,1])
C0014672 (UMLS CUI [1,2])
C2985394 (UMLS CUI [1,3])
treatment change
Item
participant had no change of treatment occur within the last 6 months;
boolean
C1299575 (UMLS CUI [1])
treatment change
Item
participants have no plans of changing to a different treatment within the next 3 months;
boolean
C1299575 (UMLS CUI [1])
informed consent
Item
participant must provide a study-specific signed informed consent form.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
3t mri contraindication
Item
patients with contraindication to 3t mri: claustrophobia, implanted metal or medical device that is not approved for mri scanning at 3t, pregnancy, inability to tolerate relative immobility for 1 hour;
boolean
C2985394 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
knee surgery, knee trauma
Item
patients with prior knee surgery or trauma of the knee;
boolean
C0187769 (UMLS CUI [1])
C0022744 (UMLS CUI [2])
kl score
Item
patients with kl score of 4.
boolean
C3177117 (UMLS CUI [1])