ID

22152

Beschreibung

MRI Markers of Cartilage Damage in Knee With Osteoarthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00820430

Link

https://clinicaltrials.gov/show/NCT00820430

Stichworte

  1. 21.05.17 21.05.17 -
Hochgeladen am

21. Mai 2017

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Osteoarthritis, Knee NCT00820430

Eligibility Osteoarthritis, Knee NCT00820430

Inclusion Criteria
Beschreibung

Inclusion Criteria

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

age

Datentyp

boolean

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

kl score

Datentyp

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);
Beschreibung

protocol specified equipment, 3t mri

Datentyp

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;
Beschreibung

treatment change

Datentyp

boolean

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

treatment change

Datentyp

boolean

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

informed consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

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;
Beschreibung

3t mri contraindication

Datentyp

boolean

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

knee surgery, knee trauma

Datentyp

boolean

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

kl score

Datentyp

boolean

Alias
UMLS CUI [1]
C3177117

Ähnliche Modelle

Eligibility Osteoarthritis, Knee NCT00820430

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])

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