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ID
12098
Beschreibung
Randomized Safety Study of CVT-301 Compared to an Observational Control Group; ODM derived from: https://clinicaltrials.gov/show/NCT02352363
Link
https://clinicaltrials.gov/show/NCT02352363
Stichworte
Versionen (2)
- 22.09.15 22.09.15 - Julian Varghese
- 22.09.15 22.09.15 - Julian Varghese
Hochgeladen am
22. September 2015
DOI
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Lizenz
Creative Commons BY-NC 3.0 Legacy
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Eligibility Idiopathic Parkinson's Disease NCT02352363
Eligibility Idiopathic Parkinson's Disease NCT02352363
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Idiopathic Parkinson's Disease NCT02352363
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Informed Consent
Item
has signed and dated an internal review board/independent ethics committee (irb/iec)-approved informed consent form before any protocol-specific screening procedures are performed.
boolean
C0021430 (UMLS CUI [1])
contraception; contraceptive; negative; screening; duration; protocol; current; serum; form; child; study; test; hcg
Item
women of child-bearing potential must use protocol-defined contraceptive measures and must have a negative serum human chorionic gonadotropin (hcg) test at screening. these patients must be willing to remain on their current form of contraception for the duration of the study.
boolean
C0700589 (UMLS CUI [1])
C1960468 (UMLS CUI [2])
C2208823 (UMLS CUI [3])
C1960468 (UMLS CUI [2])
C2208823 (UMLS CUI [3])
united kingdom; diseases; other; brain; drugs; age
Item
patients who have idiopathic pd (i.e., not induced by drugs or other diseases) as defined by fulfilling steps 1 and 2 of the united kingdom (uk) brain bank criteria, diagnosed after the age of 30 years.
boolean
C0747270 (UMLS CUI [1])
severity; staging; stage; state
Item
patients who are classified as stage 1 to 3 (in the on state) on the modified hoehn and yahr scale for staging of pd severity.
boolean
C3639483 (UMLS CUI [1])
screening; confirmed; daily; motor; time; self; day; per
Item
patients who have experienced motor fluctuations for a minimum of 2 hours of average daily off time per waking day (excluding early morning off time) by self-report and confirmed by the pd diary (on 3 consecutive days) during the screening period.
boolean
C1868976 (UMLS CUI [1])
procedure(s); procedures; severity; study
Item
patients who have dyskinesia of a severity that would significantly interfere with their ability to participate or perform study procedures.
boolean
C0013384 (UMLS CUI [1,1])
C0439793 (UMLS CUI [1,2])
C0439793 (UMLS CUI [1,2])
pregnant or lactating females
Item
pregnant or lactating females or females wishing to become pregnant.
boolean
C2828358 (UMLS CUI [1])
C0549206 (UMLS CUI [2])
C0549206 (UMLS CUI [2])
malignant melanoma; glaucoma; levodopa
Item
patients who have any known contraindication to the use of levodopa (ld), including a history of malignant melanoma or a history of narrow-angle glaucoma.
boolean
C0023570 (UMLS CUI [1,1])
C0522473 (UMLS CUI [1,2])
C0025202 (UMLS CUI [2])
C0017605 (UMLS CUI [3])
C0522473 (UMLS CUI [1,2])
C0025202 (UMLS CUI [2])
C0017605 (UMLS CUI [3])
transplantation; not limited; surgery; brain
Item
patients who have had previous surgery for pd (including but not limited to deep brain stimulation [dbs] or cell transplantation).
boolean
C0038894 (UMLS CUI [1,1])
C0030567 (UMLS CUI [1,2])
C0030567 (UMLS CUI [1,2])
anti-depressant; medications; treatment; screening; symptoms; suicide; stable; visit; dose; low
Item
patients with a history of psychotic symptoms requiring treatment, or suicide ideation or attempt within the prior 12 months (stable regimens [for at least 4 weeks prior to screening visit 1 (sv1)] of anti-depressant and certain low-dose atypical antipsychotic medications are permitted).
boolean
C0871189 (UMLS CUI [1])
C1821181 (UMLS CUI [2])
C1821181 (UMLS CUI [2])
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