ID

13303

Beschrijving

Effects of Monoamine Reuptake Inhibitor NS2330 in Parkinson's Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00006077

Link

https://clinicaltrials.gov/show/NCT00006077

Trefwoorden

Versies (1)
  1. 01-02-16 01-02-16 -
Geüploaded op

1 februari 2016

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Parkinson's Disease NCT00006077

Engels

Eligibility Parkinson's Disease NCT00006077

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
male and females are eligible for this study.
Beschrijving

gender

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
ages 18-75.
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
women must be at least one year post-menopausal or using an adequate contraceptive method for at least one month prior to and during participation in the study.
Beschrijving

menopause, contraception

Datatype

boolean

Alias
UMLS CUI [1]
C0025320
UMLS CUI [2]
C0700589
all will carry the diagnosis of idiopathic parkinson's disease based on the presence of a characteristic clinical history and neurologic findings.
Beschrijving

idiopathic parkinson

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030567
UMLS CUI [1,2]
C0332240
all will have relatively advanced disease with levodopa-associated motor response complications, including wearing-off fluctuations and peak-dose dyskinesias.
Beschrijving

disease stage

Datatype

boolean

Alias
UMLS CUI [1]
C0699749
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
the presence or history of any medical condition that can reasonably be expected to subject the patient to unwarranted risk.
Beschrijving

comorbidity

Datatype

boolean

Alias
UMLS CUI [1]
C0009488
any clinically significant laboratory abnormalities including liver enzyme elevations more than twice the upper limit of normal, or neutropenia (wbc less than 4000).
Beschrijving

laboratory test

Datatype

boolean

Alias
UMLS CUI [1]
C0022885
patients with diphasic or end-of dose dyskinesias or disabling dystonia.
Beschrijving

dyskinesia, dystonia

Datatype

boolean

Alias
UMLS CUI [1]
C0013384
UMLS CUI [2]
C0013421
patients who are unable to be treated with levodopa/carbidopa alone or a single, relatively short-acting dopamine agonist.
Beschrijving

dopa, dopa agonists

Datatype

boolean

Alias
UMLS CUI [1]
C0178601
UMLS CUI [2]
C0023570
patients with any form of parkinsonism other than idiopathic pd or with a diagnosis of dementia or major psychiatric disorder. individuals with mild to moderate depression will be sought for this study, unless their depressive disorder currently requires regular medical therapy.
Beschrijving

secondary parkinson, dementia, mental disorders

Datatype

boolean

Alias
UMLS CUI [1]
C0030569
UMLS CUI [2]
C0497327
UMLS CUI [3]
C0004936
patients who are on unacceptable prior/concomitant medications.
Beschrijving

medication

Datatype

boolean

Alias
UMLS CUI [1]
C0013227
pregnant women
Beschrijving

pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
those who are not practicing effective birth control.
Beschrijving

contraception

Datatype

boolean

Alias
UMLS CUI [1]
C0700589
patients with prior bilateral neurosurgical intervention for the treatment of parkinsonian symptoms, i.e. deep brain stimulation, pallidotomy, fetal tissue transplantation as well as patients at risk for symptomatic hypotension, cardiac arrhythmia, and/or myocardial ischemia secondary to intravenous levodopa challenge or ns2330 therapy.
Beschrijving

neurosurgery, risk factors

Datatype

boolean

Alias
UMLS CUI [1]
C0524850
UMLS CUI [2]
C0035648
patients who have taken an investigational drug within the last two months prior to randomization.
Beschrijving

study subject participation status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
previous participation in any ns 2330 study.
Beschrijving

study subject participation status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Parkinson's Disease NCT00006077

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
gender
Item
male and females are eligible for this study.
boolean
C0079399 (UMLS CUI [1])
age
Item
ages 18-75.
boolean
C0001779 (UMLS CUI [1])
menopause, contraception
Item
women must be at least one year post-menopausal or using an adequate contraceptive method for at least one month prior to and during participation in the study.
boolean
C0025320 (UMLS CUI [1])
C0700589 (UMLS CUI [2])
idiopathic parkinson
Item
all will carry the diagnosis of idiopathic parkinson's disease based on the presence of a characteristic clinical history and neurologic findings.
boolean
C0030567 (UMLS CUI [1,1])
C0332240 (UMLS CUI [1,2])
disease stage
Item
all will have relatively advanced disease with levodopa-associated motor response complications, including wearing-off fluctuations and peak-dose dyskinesias.
boolean
C0699749 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
comorbidity
Item
the presence or history of any medical condition that can reasonably be expected to subject the patient to unwarranted risk.
boolean
C0009488 (UMLS CUI [1])
laboratory test
Item
any clinically significant laboratory abnormalities including liver enzyme elevations more than twice the upper limit of normal, or neutropenia (wbc less than 4000).
boolean
C0022885 (UMLS CUI [1])
dyskinesia, dystonia
Item
patients with diphasic or end-of dose dyskinesias or disabling dystonia.
boolean
C0013384 (UMLS CUI [1])
C0013421 (UMLS CUI [2])
dopa, dopa agonists
Item
patients who are unable to be treated with levodopa/carbidopa alone or a single, relatively short-acting dopamine agonist.
boolean
C0178601 (UMLS CUI [1])
C0023570 (UMLS CUI [2])
secondary parkinson, dementia, mental disorders
Item
patients with any form of parkinsonism other than idiopathic pd or with a diagnosis of dementia or major psychiatric disorder. individuals with mild to moderate depression will be sought for this study, unless their depressive disorder currently requires regular medical therapy.
boolean
C0030569 (UMLS CUI [1])
C0497327 (UMLS CUI [2])
C0004936 (UMLS CUI [3])
medication
Item
patients who are on unacceptable prior/concomitant medications.
boolean
C0013227 (UMLS CUI [1])
pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
contraception
Item
those who are not practicing effective birth control.
boolean
C0700589 (UMLS CUI [1])
neurosurgery, risk factors
Item
patients with prior bilateral neurosurgical intervention for the treatment of parkinsonian symptoms, i.e. deep brain stimulation, pallidotomy, fetal tissue transplantation as well as patients at risk for symptomatic hypotension, cardiac arrhythmia, and/or myocardial ischemia secondary to intravenous levodopa challenge or ns2330 therapy.
boolean
C0524850 (UMLS CUI [1])
C0035648 (UMLS CUI [2])
study subject participation status
Item
patients who have taken an investigational drug within the last two months prior to randomization.
boolean
C2348568 (UMLS CUI [1])
study subject participation status
Item
previous participation in any ns 2330 study.
boolean
C2348568 (UMLS CUI [1])
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