Age
Item
aged 18 - 90
boolean
C0001779 (UMLS CUI [1])
Interphalangeal osteoarthritis
Item
definite diagnosis of ipj osteoarthritis (american college of rheumatology criteria for oa)
boolean
C0263779 (UMLS CUI [1])
Radiography of hand | Change Consistent with Osteoarthritis
Item
a previous radiograph of the hands with changes consistent with oa
boolean
C0203244 (UMLS CUI [1])
C0392747 (UMLS CUI [2,1])
C0332290 (UMLS CUI [2,2])
C0029408 (UMLS CUI [2,3])
Intervention Group | Interphalangeal joint Symptomatic Quantity | Average Severity of Pain Numeric Pain Scale | Osteoarthritis Diagnostic radiologic examination | Radial deviation Joint Degree Quantity | Ulnar deviation Joint Degree Quantity | Clinical examination | Radiology
Item
either, intervention group: at least 2 'affected' ipjs (symptomatic (>2/10 average pain on 0-10 scale in past week) and radiological oa associated with 10 degrees of either radial or ulnar deviation of the joint evident clinically and on xray)
boolean
C2986530 (UMLS CUI [1])
C0016125 (UMLS CUI [2,1])
C0231220 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C3641836 (UMLS CUI [3,1])
C1518471 (UMLS CUI [3,2])
C0029408 (UMLS CUI [4,1])
C0043299 (UMLS CUI [4,2])
C0449751 (UMLS CUI [5,1])
C0022417 (UMLS CUI [5,2])
C0449286 (UMLS CUI [5,3])
C1265611 (UMLS CUI [5,4])
C0449752 (UMLS CUI [6,1])
C0022417 (UMLS CUI [6,2])
C0449286 (UMLS CUI [6,3])
C1265611 (UMLS CUI [6,4])
C1456356 (UMLS CUI [7])
C0034571 (UMLS CUI [8])
Control Group | Interphalangeal joint Symptomatic Quantity | Average Severity of Pain Numeric Pain Scale | Osteoarthritis Diagnostic radiologic examination | Radial deviation Joint Degree Quantity | Ulnar deviation Joint Degree Quantity | Clinical examination | Radiology
Item
or control group: at least 1 'affected' ipj (symptomatic (>2/10 average pain on 0-10 scale in past week) and radiological oa associated with 10 degrees of either radial or ulnar deviation of the joint evident clinically and on x-ray)
boolean
C0009932 (UMLS CUI [1])
C0016125 (UMLS CUI [2,1])
C0231220 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C3641836 (UMLS CUI [3,1])
C1518471 (UMLS CUI [3,2])
C0029408 (UMLS CUI [4,1])
C0043299 (UMLS CUI [4,2])
C0449751 (UMLS CUI [5,1])
C0022417 (UMLS CUI [5,2])
C0449286 (UMLS CUI [5,3])
C1265611 (UMLS CUI [5,4])
C0449752 (UMLS CUI [6,1])
C0022417 (UMLS CUI [6,2])
C0449286 (UMLS CUI [6,3])
C1265611 (UMLS CUI [6,4])
C1456356 (UMLS CUI [7])
C0034571 (UMLS CUI [8])
Therapy Oral Stable | Anti-Inflammatory Agents, Non-Steroidal
Item
stable oral therapy for month prior to study entry e.g. nsaids
boolean
C0087111 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0003211 (UMLS CUI [2])
Informed Consent
Item
capable of providing written informed consent
boolean
C0021430 (UMLS CUI [1])
Medical contraindication Splinting | Hypersensitivity Materials
Item
contraindication to splinting e.g. allergy to materials
boolean
C1301624 (UMLS CUI [1,1])
C2014585 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0520510 (UMLS CUI [2,2])
Operative Surgical Procedure Planned
Item
planned surgery during study period
boolean
C0543467 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
Steroids Oral | Steroids Intramuscular | Steroids Intraarticular
Item
oral, intramuscular or intraarticular steroids within 3 months of study entry
boolean
C0038317 (UMLS CUI [1,1])
C1527415 (UMLS CUI [1,2])
C0038317 (UMLS CUI [2,1])
C1556154 (UMLS CUI [2,2])
C0038317 (UMLS CUI [3,1])
C1522204 (UMLS CUI [3,2])
Hyaluronic Acid Intraarticular Interphalangeal joint
Item
intraarticular hyaluronans to any nominated ip joints within 6 months of study entry
boolean
C0020196 (UMLS CUI [1,1])
C1522204 (UMLS CUI [1,2])
C0016125 (UMLS CUI [1,3])
Residence Except UK
Item
not resident in uk
boolean
C0237096 (UMLS CUI [1,1])
C0332300 (UMLS CUI [1,2])
C0041700 (UMLS CUI [1,3])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Arthritis
Item
other inflammatory arthritis
boolean
C0003864 (UMLS CUI [1])
Psoriasis
Item
history of psoriasis
boolean
C0033860 (UMLS CUI [1])
Study Subject Participation Status | Interventional Study
Item
participation in other intervention trials
boolean
C2348568 (UMLS CUI [1])
C3274035 (UMLS CUI [2])
Medical Problem Uncontrolled | Medical Problem Severe | Study Subject Participation Status Inappropriate
Item
patients with any uncontrolled or severe medical problems which in the opinion of the investigator makes them unsuitable for study participation
boolean
C1254481 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C1254481 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C2348568 (UMLS CUI [3,1])
C1548788 (UMLS CUI [3,2])
Informed Consent English Language Unable
Item
unable to give informed written consent in english
boolean
C0021430 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])