Eligibility Osteoarthritis NCT02044432

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
chronic osteoarthritis, mainly osteoarthritis of the knee
Description

Chronic osteoarthritis | Knee Osteoarthritis predominant

Data type

boolean

Alias
UMLS CUI [1]
C0263778
UMLS CUI [2,1]
C0409959
UMLS CUI [2,2]
C1542147
osteoarthritis symptoms for at least six months
Description

Osteoarthritis Symptoms Duration

Data type

boolean

Alias
UMLS CUI [1,1]
C0029408
UMLS CUI [1,2]
C1457887
UMLS CUI [1,3]
C0449238
written consent to participate in the study
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
age: 30 years and more
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
rheumatoid arthritis
Description

Rheumatoid Arthritis

Data type

boolean

Alias
UMLS CUI [1]
C0003873
fibromyalgia
Description

Fibromyalgia

Data type

boolean

Alias
UMLS CUI [1]
C0016053
oncological or other serious diseases
Description

Malignant disease | Disease Serious

Data type

boolean

Alias
UMLS CUI [1]
C0442867
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C0205404
use of corticosteroids
Description

Adrenal Cortex Hormones

Data type

boolean

Alias
UMLS CUI [1]
C0001617
nephropathy
Description

Kidney Disease

Data type

boolean

Alias
UMLS CUI [1]
C0022658
non-intact skin conditions in the area of application
Description

Impaired skin integrity Site Application

Data type

boolean

Alias
UMLS CUI [1,1]
C4048181
UMLS CUI [1,2]
C1515974
UMLS CUI [1,3]
C0185125
hypersensitivity / allergy to ginger
Description

Hypersensitivity Ginger

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0162751
simultaneous participation in another clinical trial
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Osteoarthritis NCT02044432

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Chronic osteoarthritis | Knee Osteoarthritis predominant
Item
chronic osteoarthritis, mainly osteoarthritis of the knee
boolean
C0263778 (UMLS CUI [1])
C0409959 (UMLS CUI [2,1])
C1542147 (UMLS CUI [2,2])
Osteoarthritis Symptoms Duration
Item
osteoarthritis symptoms for at least six months
boolean
C0029408 (UMLS CUI [1,1])
C1457887 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Informed Consent
Item
written consent to participate in the study
boolean
C0021430 (UMLS CUI [1])
Age
Item
age: 30 years and more
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Rheumatoid Arthritis
Item
rheumatoid arthritis
boolean
C0003873 (UMLS CUI [1])
Fibromyalgia
Item
fibromyalgia
boolean
C0016053 (UMLS CUI [1])
Malignant disease | Disease Serious
Item
oncological or other serious diseases
boolean
C0442867 (UMLS CUI [1])
C0012634 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
Adrenal Cortex Hormones
Item
use of corticosteroids
boolean
C0001617 (UMLS CUI [1])
Kidney Disease
Item
nephropathy
boolean
C0022658 (UMLS CUI [1])
Impaired skin integrity Site Application
Item
non-intact skin conditions in the area of application
boolean
C4048181 (UMLS CUI [1,1])
C1515974 (UMLS CUI [1,2])
C0185125 (UMLS CUI [1,3])
Hypersensitivity Ginger
Item
hypersensitivity / allergy to ginger
boolean
C0020517 (UMLS CUI [1,1])
C0162751 (UMLS CUI [1,2])
Study Subject Participation Status
Item
simultaneous participation in another clinical trial
boolean
C2348568 (UMLS CUI [1])