ID

34443

Description

Ultrasound Guided vs Unguided Intra-articular Knee Injections; ODM derived from: https://clinicaltrials.gov/show/NCT02092246

Link

https://clinicaltrials.gov/show/NCT02092246

Keywords

  1. 1/17/19 1/17/19 -
Copyright Holder

see on clinicaltrials.gov

Uploaded on

January 17, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Osteoarthritis NCT02092246

Eligibility Osteoarthritis NCT02092246

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
bmi > 30
Description

ID.1

Data type

boolean

no clinically detectable knee effusion
Description

ID.2

Data type

boolean

clinical or radiographic evidence of knee osteoarthritis or inflammatory arthritis
Description

ID.3

Data type

boolean

must be referred to the pain clinic for treatment
Description

ID.4

Data type

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of surgery on the affected knee
Description

ID.5

Data type

boolean

evidence of untreated systemic infection or systemic immunocompromise
Description

ID.6

Data type

boolean

evidence of cutaneous infections near the study knee injection site
Description

ID.7

Data type

boolean

patients on warfarin with an inr > 3.0
Description

ID.8

Data type

boolean

patients on oral antiplatelet or anticoagulant medications will be excluded if they have documented evidence of renal insufficiency (gfr < 60)
Description

ID.9

Data type

boolean

history of iodinated contrast allergy or significant reaction to corticosteroids or lidocaine
Description

ID.10

Data type

boolean

Similar models

Eligibility Osteoarthritis NCT02092246

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
bmi > 30
boolean
ID.2
Item
no clinically detectable knee effusion
boolean
ID.3
Item
clinical or radiographic evidence of knee osteoarthritis or inflammatory arthritis
boolean
ID.4
Item
must be referred to the pain clinic for treatment
boolean
Item Group
C0680251 (UMLS CUI)
ID.5
Item
history of surgery on the affected knee
boolean
ID.6
Item
evidence of untreated systemic infection or systemic immunocompromise
boolean
ID.7
Item
evidence of cutaneous infections near the study knee injection site
boolean
ID.8
Item
patients on warfarin with an inr > 3.0
boolean
ID.9
Item
patients on oral antiplatelet or anticoagulant medications will be excluded if they have documented evidence of renal insufficiency (gfr < 60)
boolean
ID.10
Item
history of iodinated contrast allergy or significant reaction to corticosteroids or lidocaine
boolean

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