Age
Item
male or female aged between 18 and 70
boolean
C0001779 (UMLS CUI [1])
Comprehension Study Protocol
Item
capable of reading and understanding the information leaflet given to him/her
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
Informed Consent
Item
signed an inform consent form
boolean
C0021430 (UMLS CUI [1])
Parkinson Disease Hoehn and Yahr Scale score
Item
presenting with idiopathic parkinson's disease with a hoehn and yahr score of ≤ 3
boolean
C0030567 (UMLS CUI [1,1])
C4274823 (UMLS CUI [1,2])
Antiparkinson Agents Absent | Levodopa Dosage | Dopamine Agonists | Exception Pramipexole
Item
has never been given anti-parkinson medication, or has been treated with l-dopa, on condition that the total duration of treatment was less than twelve weeks at a dosage of under 200 mg, or has been treated with a dopamine agonist other than pramipexole, on condition that:
boolean
C0003405 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0023570 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0178601 (UMLS CUI [3])
C1705847 (UMLS CUI [4,1])
C0074710 (UMLS CUI [4,2])
Dosage Titration Phase
Item
either the patient is still in the dose-titration phase at the time of inclusion
boolean
C0178602 (UMLS CUI [1,1])
C0162621 (UMLS CUI [1,2])
C0205390 (UMLS CUI [1,3])
Duration of treatment | Treatment completed
Item
or that the treatment was administered for less than six weeks and was completed two weeks before inclusion
boolean
C0444921 (UMLS CUI [1])
C0580352 (UMLS CUI [2])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
women who are pregnant, breastfeeding, or planning a pregnancy in the months after joining the study
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Childbearing Potential Female Sterilization Absent | Childbearing Potential Contraceptive methods Absent
Item
women of reproductive age who have not undergone surgical sterilisation or who are not using a reliable method of contraception before joining the study and during the study
boolean
C3831118 (UMLS CUI [1,1])
C0015787 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Hepatic Insufficiency
Item
patient presenting with hepatic insufficiency
boolean
C1306571 (UMLS CUI [1])
Comorbidity Significant Medical History | Comorbidity Significant Medical Examination
Item
patient presenting with a concommitant illness which is considered significant by the investigator, after examination of the history, the patient's clinical condition, or on the basis on any additional examinations performed
boolean
C0009488 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
C0262926 (UMLS CUI [1,3])
C0009488 (UMLS CUI [2,1])
C0750502 (UMLS CUI [2,2])
C0582103 (UMLS CUI [2,3])
Skin lesion Suspect | Evaluation Lacking
Item
patient presenting with a skin lesion considered to be suspect by the investigator and which has not been evaluated by a dermatologist
boolean
C0037284 (UMLS CUI [1,1])
C0750491 (UMLS CUI [1,2])
C1261322 (UMLS CUI [2,1])
C0332268 (UMLS CUI [2,2])
Medical contraindication rasagiline | Medical contraindication Pramipexole
Item
patient presenting with a contraindication to treatment with rasagiline or pramipexole (please see the spc for the respective products)
boolean
C1301624 (UMLS CUI [1,1])
C0525678 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0074710 (UMLS CUI [2,2])
Fluoxetine
Item
patient treated with fuoxetine during the five weeks preceding inclusion
boolean
C0016365 (UMLS CUI [1])
Fluvoxamine | Meperidine | Selegiline | Monoamine Oxidase Inhibitors
Item
patient treated with fluvoxamine, pethidine, selegiline or any other maoi during the two weeks preceding inclusion
boolean
C0085228 (UMLS CUI [1])
C0025376 (UMLS CUI [2])
C0036579 (UMLS CUI [3])
C0026457 (UMLS CUI [4])
Deep Brain Stimulation
Item
patient who has had deep brain stimulation treatment
boolean
C0394162 (UMLS CUI [1])
Dextromethorphan | Sympathomimetics
Item
patient who might receive dextromethorphan or a sympathomimetic during the study
boolean
C0011816 (UMLS CUI [1])
C0039052 (UMLS CUI [2])