ID.1
Item
male or female patients aged 40 years or over.
boolean
C0001779 (UMLS CUI [1])
ID.2
Item
body mass index (bmi) of 35 or less.
boolean
C1305855 (UMLS CUI [1])
ID.3
Item
history of oa of the knee for at least 1 year and has experienced pain in the target area for at least six months.
boolean
C0409959 (UMLS CUI [1])
ID.4
Item
x-ray of the target knee.
boolean
C0203273 (UMLS CUI [1])
ID.5
Item
willing and able to complete the study procedures.
boolean
C0021430 (UMLS CUI [1])
ID.6
Item
female patients who are pregnant or lactating or who plan to get pregnant.
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
ID.7
Item
clinically significant form of joint disease other than oa.
boolean
C0022408 (UMLS CUI [1])
ID.8
Item
medical condition that could adversely impact the patient's participation, safety or affect the conduct of the study.
boolean
C0012634 (UMLS CUI [1])
ID.9
Item
prior major trauma in the target knee or major surgeries such as partial or total knee arthroplasty.
boolean
C0332677 (UMLS CUI [1,1])
C0679637 (UMLS CUI [1,2])
C0022742 (UMLS CUI [1,3])
ID.10
Item
arthroscopic surgery on the target knee within 6 months.
boolean
C0022742 (UMLS CUI [1,1])
C0750934 (UMLS CUI [1,2])