Parkinson's disease and hoehn and yahr scale
Item
patients diagnosed with idiopathic parkinson's disease and classified as stage ii-iv of the hoehn and yahr scale for staging the severity of parkinson's disease
boolean
C0030567 (UMLS CUI [1])
C0451215 (UMLS CUI [2])
Pharmacotherapy regimen
Item
patients must have been on an optimally maximized oral therapy regimen including levodopa/decarboxylase inhibitors in either immediate or delayed release forms, plus at least one direct acting oral dopamine agonist for at least 30 days prior to randomization
boolean
C0023570 (UMLS CUI [1])
C0360140 (UMLS CUI [2])
C0178601 (UMLS CUI [3])
Apomorphine subcutaneous injections dosage
Item
patients must have been receiving apomorphine subcutaneous injections for rescue therapy for "off" events for at least three months with an average dosing requirement of at least 2 doses per day over the week prior to enrollment with a dose of less than 11 mg
boolean
C0003596 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Medical therapy for psychoses or dementia
Item
patients under medical therapy for clinically significant psychoses or dementia not related to ingestion of antiparkinson medications. (patients with hallucinations or other central adverse reactions associated solely with antiparkinson medications were not excluded.)
boolean
C0418981 (UMLS CUI [1,1])
C0033975 (UMLS CUI [1,2])
C0418981 (UMLS CUI [2,1])
C0497327 (UMLS CUI [2,2])
Substance use disorder
Item
patients with a history of drug or alcohol dependency within one year prior to study enrollment
boolean
C0038586 (UMLS CUI [1])
Comorbidity
Item
patients with unstable and clinically significant disease of cardiovascular (including orthostatic hypotension), hematologic (including coombs' positive hemolytic anemia), hepatic, renal, metabolic, respiratory, gastrointestinal or endocrinological systems or neoplasm within the threemonths before the start of the study.
boolean
C0009488 (UMLS CUI [1])
Allergy to pharmacotherapy
Item
patients with a history of allergy or intolerance to morphine or its derivatives, sulfur, sulfur containing medication, sulfites, domperidone, trimethobenzamide or other anticholinergics.
boolean
C0020517 (UMLS CUI [1,1])
C0013216 (UMLS CUI [1,2])
Experimental drug
Item
patients treated with experimental agents (other than apomorphine intermittent subcutaneous injections) within 3 months before study entry, experimental agents were defined on the basis of the regulatory status in the country of patient observation, or with other disallowed medications
boolean
C0304229 (UMLS CUI [1])
Apomorphine regimen
Item
patients whose apomorphine regimen was characterized by continuous infusion or by administration methods other than intermittent subcutaneous injection.
boolean
C0003596 (UMLS CUI [1,1])
C0040808 (UMLS CUI [1,2])
Informed consent
Item
patients who could not or would not sign an informed consent form.
boolean
C0021430 (UMLS CUI [1])