A Biospecimen and Clinical Data Study on Patients for Drug & Biomarker Discovery
NCT ID: NCT01592552
Last Updated: 2023-11-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
20 participants
OBSERVATIONAL
2011-11-30
2015-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
CROSS_SECTIONAL
Study Groups
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Neurological Condition
Collect blood and other biospecimens like saliva, urine and CSF for research purposes.
No interventions assigned to this group
Control
Collect blood and other biospecimens like saliva, urine and CSF for research purposes.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* A diagnosis of neurological condition
* Proof of diagnosis can be provided
Control group: Healthy donors, males and females, 18 to 100 years of age
Exclusion Criteria
* Receipt of an investigational (unapproved) drug within 30 days of study enrollment
18 Years
100 Years
ALL
Yes
Sponsors
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Sanguine Biosciences
INDUSTRY
Responsible Party
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Principal Investigators
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Phil Silkoff, MD
Role: PRINCIPAL_INVESTIGATOR
Sanguine Biosciences
Locations
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Sanguine Biosciences
Sherman Oaks, California, United States
Countries
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Other Identifiers
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SAN-ND-01
Identifier Type: -
Identifier Source: org_study_id