ID

24889

Description

Clinical Effects of Vitamin D Repletion in Patients With Parkinson's Disease; ODM derived from: https://clinicaltrials.gov/show/NCT00571285

Link

https://clinicaltrials.gov/show/NCT00571285

Keywords

Versions (1)
  1. 8/22/17 8/22/17 -
Uploaded on

August 22, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Parkinson's Disease NCT00571285

English

Eligibility Parkinson's Disease NCT00571285

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
eligible participants must be able to provide informed consent or have a legal representative (defined by georgia law) who can give consent.
Description

Informed Consent | Informed Consent Patient Representative

Data type

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0030701
diagnosis of ipd, based on history of 2/3 cardinal features of pd (tremor, bradykinesia and rigidity) and definite response to dopaminergic therapy.
Description

Parkinson Disease | Tremor | Bradykinesia | Rigidity | Dopamine Agonists Good therapeutic response

Data type

boolean

Alias
UMLS CUI [1]
C0030567
UMLS CUI [2]
C0040822
UMLS CUI [3]
C0233565
UMLS CUI [4]
C0026837
UMLS CUI [5,1]
C0178601
UMLS CUI [5,2]
C0184785
previous serum 25-oh vitamin d concentration measured by treating physician within previous 3 months.
Description

25-Oh D Vitamin Test

Data type

boolean

Alias
UMLS CUI [1]
C1255280
eligible participants must be able to complete the study questionnaires and assessments (e.g., participant must be judged able to complete tug at screening/baseline).
Description

Clinical Trial Subject Questionnaire Completion | TUG Completion

Data type

boolean

Alias
UMLS CUI [1,1]
C3890411
UMLS CUI [1,2]
C0205197
UMLS CUI [2,1]
C1319201
UMLS CUI [2,2]
C0205197
participants must be free of active cancer or other serious medical condition which might reasonably preclude their completing the 6-month intervention.
Description

Malignant Neoplasm Free of | Medical condition Serious Free of

Data type

boolean

Alias
UMLS CUI [1,1]
C0006826
UMLS CUI [1,2]
C0332296
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C0205404
UMLS CUI [2,3]
C0332296
participants must be able to complete an 8 meter walk at screening evaluation.
Description

Able to walk Meter Quantity

Data type

boolean

Alias
UMLS CUI [1,1]
C2712089
UMLS CUI [1,2]
C0475209
UMLS CUI [1,3]
C1265611
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with pd, h&y stage i-iv will be eligible to participate in this study.
Description

Parkinson Disease Hoehn and Yahr grades

Data type

boolean

Alias
UMLS CUI [1,1]
C0030567
UMLS CUI [1,2]
C0451215
participants must be ages 18-89 years.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patient with a history of hypercalcemia, hypercalciuria, liver failure, end-stage renal disease (national kidney foundation classification stage 5) or kidney stones within the past 5 years will be excluded.
Description

Hypercalcemia | Hypercalciuria | Liver Failure | Chronic Kidney Failure Chronic kidney disease NKF classification | Kidney Calculi

Data type

boolean

Alias
UMLS CUI [1]
C0020437
UMLS CUI [2]
C0020438
UMLS CUI [3]
C0085605
UMLS CUI [4,1]
C0022661
UMLS CUI [4,2]
C2074730
UMLS CUI [5]
C0022650
specifically, potential participants with gfr (estimated or measured) <15 ml/min are excluded.
Description

Estimated Glomerular Filtration Rate | Glomerular Filtration Rate

Data type

boolean

Alias
UMLS CUI [1]
C3811844
UMLS CUI [2]
C0017654
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Similar models

Eligibility Parkinson's Disease NCT00571285

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent | Informed Consent Patient Representative
Item
eligible participants must be able to provide informed consent or have a legal representative (defined by georgia law) who can give consent.
boolean
C0021430 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C0030701 (UMLS CUI [2,2])
Parkinson Disease | Tremor | Bradykinesia | Rigidity | Dopamine Agonists Good therapeutic response
Item
diagnosis of ipd, based on history of 2/3 cardinal features of pd (tremor, bradykinesia and rigidity) and definite response to dopaminergic therapy.
boolean
C0030567 (UMLS CUI [1])
C0040822 (UMLS CUI [2])
C0233565 (UMLS CUI [3])
C0026837 (UMLS CUI [4])
C0178601 (UMLS CUI [5,1])
C0184785 (UMLS CUI [5,2])
25-Oh D Vitamin Test
Item
previous serum 25-oh vitamin d concentration measured by treating physician within previous 3 months.
boolean
C1255280 (UMLS CUI [1])
Clinical Trial Subject Questionnaire Completion | TUG Completion
Item
eligible participants must be able to complete the study questionnaires and assessments (e.g., participant must be judged able to complete tug at screening/baseline).
boolean
C3890411 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C1319201 (UMLS CUI [2,1])
C0205197 (UMLS CUI [2,2])
Malignant Neoplasm Free of | Medical condition Serious Free of
Item
participants must be free of active cancer or other serious medical condition which might reasonably preclude their completing the 6-month intervention.
boolean
C0006826 (UMLS CUI [1,1])
C0332296 (UMLS CUI [1,2])
C3843040 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C0332296 (UMLS CUI [2,3])
Able to walk Meter Quantity
Item
participants must be able to complete an 8 meter walk at screening evaluation.
boolean
C2712089 (UMLS CUI [1,1])
C0475209 (UMLS CUI [1,2])
C1265611 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Parkinson Disease Hoehn and Yahr grades
Item
patients with pd, h&y stage i-iv will be eligible to participate in this study.
boolean
C0030567 (UMLS CUI [1,1])
C0451215 (UMLS CUI [1,2])
Age
Item
participants must be ages 18-89 years.
boolean
C0001779 (UMLS CUI [1])
Hypercalcemia | Hypercalciuria | Liver Failure | Chronic Kidney Failure Chronic kidney disease NKF classification | Kidney Calculi
Item
patient with a history of hypercalcemia, hypercalciuria, liver failure, end-stage renal disease (national kidney foundation classification stage 5) or kidney stones within the past 5 years will be excluded.
boolean
C0020437 (UMLS CUI [1])
C0020438 (UMLS CUI [2])
C0085605 (UMLS CUI [3])
C0022661 (UMLS CUI [4,1])
C2074730 (UMLS CUI [4,2])
C0022650 (UMLS CUI [5])
Estimated Glomerular Filtration Rate | Glomerular Filtration Rate
Item
specifically, potential participants with gfr (estimated or measured) <15 ml/min are excluded.
boolean
C3811844 (UMLS CUI [1])
C0017654 (UMLS CUI [2])
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