Chronic pain Duration | Etiology Knee Osteoarthritis | Etiology Osteoarthritis of hip
Item
patients who complain of chronic pain caused by osteoarthritis of the knee or hip persisting for 3 months or longer
boolean
C0150055 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0015127 (UMLS CUI [2,1])
C0409959 (UMLS CUI [2,2])
C0015127 (UMLS CUI [3,1])
C0029410 (UMLS CUI [3,2])
Protocol Compliance | Other Coding
Item
patients who can fully observe the overall clinical study requirements including k-womac completion at the investigator's discretion
boolean
C0525058 (UMLS CUI [1])
C3846158 (UMLS CUI [2])
Severe pain Numeric Pain Scale | Analgesic therapy Inadequate
Item
patients who complain of severe pain (nrs score = 7) because pain was not treated enough with the previous analgesic
boolean
C0278140 (UMLS CUI [1,1])
C1518471 (UMLS CUI [1,2])
C0412784 (UMLS CUI [2,1])
C0205412 (UMLS CUI [2,2])
Opioid Analgesics Strong Absent
Item
patients who have never been administered strong opioid analgesics over the last one month
boolean
C0002772 (UMLS CUI [1,1])
C0442821 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
Substance Use Disorders
Item
patients with a history of the drug or alcohol abuse in the past or now
boolean
C0038586 (UMLS CUI [1])
Childbearing Potential Pregnancy | Childbearing Potential Pregnancy Probably | Gender Fertility | Gender Sexual Abstinence Unwilling | Partner Contraceptive methods Absent | Contraceptive implant | Contraceptive injection | Contraceptives, Oral | Intrauterine Devices
Item
childbearing women who are pregnant or likely to be pregnant during the study period and male subjects who are neither infertile nor willing to refrain from sexual relations but whose partner does not conduct an effective contraception (implant, injections, oral contraceptives, intrauterine device, etc.)
boolean
C3831118 (UMLS CUI [1,1])
C0032961 (UMLS CUI [1,2])
C3831118 (UMLS CUI [2,1])
C0032961 (UMLS CUI [2,2])
C0750492 (UMLS CUI [2,3])
C0079399 (UMLS CUI [3,1])
C0015895 (UMLS CUI [3,2])
C0079399 (UMLS CUI [4,1])
C0036899 (UMLS CUI [4,2])
C0558080 (UMLS CUI [4,3])
C0682323 (UMLS CUI [5,1])
C0700589 (UMLS CUI [5,2])
C0332197 (UMLS CUI [5,3])
C1657106 (UMLS CUI [6])
C1656586 (UMLS CUI [7])
C0009905 (UMLS CUI [8])
C0021900 (UMLS CUI [9])
Use of Transdermal System Unable | Transdermal System Due to Dermatologic disorders
Item
patients who are unable to use a transdermal system due to skin disease
boolean
C1524063 (UMLS CUI [1,1])
C0991556 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0991556 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0037274 (UMLS CUI [2,3])
Serious mental illness
Item
patients with serious mental disorder
boolean
C3841614 (UMLS CUI [1])
Opioid analgesic allergy
Item
patients with history of hypersensitivity to opioid analgesics
boolean
C0570515 (UMLS CUI [1])
Hypercapnia
Item
patients with history of co2 retention
boolean
C0020440 (UMLS CUI [1])
Study Subject Participation Status Ineligible | Etiology Pharmaceutical Product Label Warning | Etiology Pharmaceutical Product Label Precaution | Etiology Pharmaceutical Product Label Medical contraindication
Item
patients who are not eligible for the study participation based on warnings, precautions and contra medications in the package insert of the study drug at the investigator's discretion
boolean
C2348568 (UMLS CUI [1,1])
C1512714 (UMLS CUI [1,2])
C0015127 (UMLS CUI [2,1])
C1705425 (UMLS CUI [2,2])
C0687677 (UMLS CUI [2,3])
C0015127 (UMLS CUI [3,1])
C1705425 (UMLS CUI [3,2])
C1882442 (UMLS CUI [3,3])
C0015127 (UMLS CUI [4,1])
C1705425 (UMLS CUI [4,2])
C1301624 (UMLS CUI [4,3])