ID

36807

Description

Treating Bacterial Overgrowth in Parkinson's Disease; ODM derived from: https://clinicaltrials.gov/show/NCT02470780

Link

https://clinicaltrials.gov/show/NCT02470780

Keywords

Versions (1)
  1. 6/11/19 6/11/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

June 11, 2019

DOI

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License

Creative Commons BY 4.0
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Eligibility Parkinson's Disease NCT02470780

English

Eligibility Parkinson's Disease NCT02470780

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
diagnosis of idiopathic pd
Description

Parkinson Disease

Data type

boolean

Alias
UMLS CUI [1]
C0030567
daily "off" time ≥ 4 hours
Description

Off Treatment hours/day

Data type

boolean

Alias
UMLS CUI [1,1]
C1518544
UMLS CUI [1,2]
C0556974
no changes in levodopa or any other dopaminergic medications expected during the course of the study
Description

Levodopa unchanged | Dopamine Agonists unchanged

Data type

boolean

Alias
UMLS CUI [1,1]
C0023570
UMLS CUI [1,2]
C0442739
UMLS CUI [2,1]
C0178601
UMLS CUI [2,2]
C0442739
will be screened for cognitive ability (montreal cognitive assessment score of ≥ 24) prior to enrollment
Description

Cognitive ability Montreal cognitive assessment

Data type

boolean

Alias
UMLS CUI [1,1]
C0392334
UMLS CUI [1,2]
C3496286
will be screened for presence of sibo prior to enrollment
Description

SIBO Screening

Data type

boolean

Alias
UMLS CUI [1,1]
C2959722
UMLS CUI [1,2]
C0220908
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
any comorbid non-pd-associated gastrointestinal (e.g., achlorhydria) or systemic diseases that may alter absorption or confound the study results
Description

Gastrointestinal Disease Changing Absorption | Gastrointestinal Disease Interferes with Research results | Absence Relationship Parkinson Disease | Achlorhydria | Systemic disease Changing Absorption | Systemic disease Interferes with Research results

Data type

boolean

Alias
UMLS CUI [1,1]
C0017178
UMLS CUI [1,2]
C0392747
UMLS CUI [1,3]
C0237442
UMLS CUI [2,1]
C0017178
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0683954
UMLS CUI [3,1]
C0332197
UMLS CUI [3,2]
C0439849
UMLS CUI [3,3]
C0030567
UMLS CUI [4]
C0001075
UMLS CUI [5,1]
C0442893
UMLS CUI [5,2]
C0392747
UMLS CUI [5,3]
C0237442
UMLS CUI [6,1]
C0442893
UMLS CUI [6,2]
C0521102
UMLS CUI [6,3]
C0683954
exposure to proton pump inhibitors, immunosuppressive drugs, medications that affect gi motility (such as prokinetics, anticholinergics, and tricyclic antidepressants), antibiotics or any other drugs that affect the intestinal flora (such as laxatives) within a month prior to enrollment.
Description

Exposure to Proton Pump Inhibitors | Exposure to Immunosuppressive Agents | Pharmaceutical Preparations Affecting Gastrointestinal Motility | Prokinetic Agent | Anticholinergic Agents | Tricyclic Antidepressive Agents | Antibiotics | Pharmaceutical Preparations Affecting Intestinal Flora | Laxatives

Data type

boolean

Alias
UMLS CUI [1,1]
C0332157
UMLS CUI [1,2]
C0358591
UMLS CUI [2,1]
C0332157
UMLS CUI [2,2]
C0021081
UMLS CUI [3,1]
C0013227
UMLS CUI [3,2]
C0392760
UMLS CUI [3,3]
C0017184
UMLS CUI [4]
C1268865
UMLS CUI [5]
C0242896
UMLS CUI [6]
C0003290
UMLS CUI [7]
C0003232
UMLS CUI [8,1]
C0013227
UMLS CUI [8,2]
C0392760
UMLS CUI [8,3]
C2985398
UMLS CUI [9]
C0282090
prior deep brain stimulation or ablative functional neurosurgery.
Description

Deep Brain Stimulation | Ablation Neurosurgical Procedure

Data type

boolean

Alias
UMLS CUI [1]
C0394162
UMLS CUI [2,1]
C0547070
UMLS CUI [2,2]
C0524850
prior allergy to rifaximin
Description

Hypersensitivity Rifaximin

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0073374
women who are pregnant, lactating, or plan to become pregnant.
Description

Pregnancy | Breast Feeding | Pregnancy, Planned

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0032992
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Similar models

Eligibility Parkinson's Disease NCT02470780

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Parkinson Disease
Item
diagnosis of idiopathic pd
boolean
C0030567 (UMLS CUI [1])
Off Treatment hours/day
Item
daily "off" time ≥ 4 hours
boolean
C1518544 (UMLS CUI [1,1])
C0556974 (UMLS CUI [1,2])
Levodopa unchanged | Dopamine Agonists unchanged
Item
no changes in levodopa or any other dopaminergic medications expected during the course of the study
boolean
C0023570 (UMLS CUI [1,1])
C0442739 (UMLS CUI [1,2])
C0178601 (UMLS CUI [2,1])
C0442739 (UMLS CUI [2,2])
Cognitive ability Montreal cognitive assessment
Item
will be screened for cognitive ability (montreal cognitive assessment score of ≥ 24) prior to enrollment
boolean
C0392334 (UMLS CUI [1,1])
C3496286 (UMLS CUI [1,2])
SIBO Screening
Item
will be screened for presence of sibo prior to enrollment
boolean
C2959722 (UMLS CUI [1,1])
C0220908 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Gastrointestinal Disease Changing Absorption | Gastrointestinal Disease Interferes with Research results | Absence Relationship Parkinson Disease | Achlorhydria | Systemic disease Changing Absorption | Systemic disease Interferes with Research results
Item
any comorbid non-pd-associated gastrointestinal (e.g., achlorhydria) or systemic diseases that may alter absorption or confound the study results
boolean
C0017178 (UMLS CUI [1,1])
C0392747 (UMLS CUI [1,2])
C0237442 (UMLS CUI [1,3])
C0017178 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0683954 (UMLS CUI [2,3])
C0332197 (UMLS CUI [3,1])
C0439849 (UMLS CUI [3,2])
C0030567 (UMLS CUI [3,3])
C0001075 (UMLS CUI [4])
C0442893 (UMLS CUI [5,1])
C0392747 (UMLS CUI [5,2])
C0237442 (UMLS CUI [5,3])
C0442893 (UMLS CUI [6,1])
C0521102 (UMLS CUI [6,2])
C0683954 (UMLS CUI [6,3])
Exposure to Proton Pump Inhibitors | Exposure to Immunosuppressive Agents | Pharmaceutical Preparations Affecting Gastrointestinal Motility | Prokinetic Agent | Anticholinergic Agents | Tricyclic Antidepressive Agents | Antibiotics | Pharmaceutical Preparations Affecting Intestinal Flora | Laxatives
Item
exposure to proton pump inhibitors, immunosuppressive drugs, medications that affect gi motility (such as prokinetics, anticholinergics, and tricyclic antidepressants), antibiotics or any other drugs that affect the intestinal flora (such as laxatives) within a month prior to enrollment.
boolean
C0332157 (UMLS CUI [1,1])
C0358591 (UMLS CUI [1,2])
C0332157 (UMLS CUI [2,1])
C0021081 (UMLS CUI [2,2])
C0013227 (UMLS CUI [3,1])
C0392760 (UMLS CUI [3,2])
C0017184 (UMLS CUI [3,3])
C1268865 (UMLS CUI [4])
C0242896 (UMLS CUI [5])
C0003290 (UMLS CUI [6])
C0003232 (UMLS CUI [7])
C0013227 (UMLS CUI [8,1])
C0392760 (UMLS CUI [8,2])
C2985398 (UMLS CUI [8,3])
C0282090 (UMLS CUI [9])
Deep Brain Stimulation | Ablation Neurosurgical Procedure
Item
prior deep brain stimulation or ablative functional neurosurgery.
boolean
C0394162 (UMLS CUI [1])
C0547070 (UMLS CUI [2,1])
C0524850 (UMLS CUI [2,2])
Hypersensitivity Rifaximin
Item
prior allergy to rifaximin
boolean
C0020517 (UMLS CUI [1,1])
C0073374 (UMLS CUI [1,2])
Pregnancy | Breast Feeding | Pregnancy, Planned
Item
women who are pregnant, lactating, or plan to become pregnant.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
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