Observational Research on Use of Immunoprop Supplement in Chronic Fatigue Syndrome
NCT ID: NCT01893619
Last Updated: 2013-07-25
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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UNKNOWN
100 participants
OBSERVATIONAL
2013-06-30
2013-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
21 Years
60 Years
ALL
No
Sponsors
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New York CFS Association
OTHER
Responsible Party
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Principal Investigators
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DEREK enlander
Role: PRINCIPAL_INVESTIGATOR
CFIDS RESEARCH FOUNDATION
Locations
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Me/Cfs Center,860 Fifth Avenue
New York, New York, United States
Countries
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Facility Contacts
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Other Identifiers
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immunoprop
Identifier Type: -
Identifier Source: org_study_id
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