A Retrospective Chart Review Study of Gene-Eden-VIR/Novirin
NCT ID: NCT02715752
Last Updated: 2016-04-26
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
1000 participants
OBSERVATIONAL
2016-01-31
2016-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Herpes Simplex Virus Infection
Gene-Eden-VIR/Novirin, oral, 1-4 capsules per day, 12 months
Gene-Eden-VIR/Novirin
Human Papillomavirus Infection
Gene-Eden-VIR/Novirin, oral, 1-4 capsules per day, 12 months
Gene-Eden-VIR/Novirin
Epstein-Barr Virus Infection
Gene-Eden-VIR/Novirin, oral, 1-4 capsules per day, 12 months
Gene-Eden-VIR/Novirin
Cytomegalovirus Infection
Gene-Eden-VIR/Novirin, oral, 1-4 capsules per day, 12 months
Gene-Eden-VIR/Novirin
Varicella Zoster Virus Infection
Gene-Eden-VIR/Novirin, oral, 1-4 capsules per day, 12 months
Gene-Eden-VIR/Novirin
Interventions
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Gene-Eden-VIR/Novirin
Eligibility Criteria
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Inclusion Criteria
* Taking Gene-Eden-VIR/Novirin
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
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The Center for the Biology of Chronic Disease
OTHER
Responsible Party
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Locations
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The Center for the Biology of Chronic Disease
Valley Cottage, New York, United States
Countries
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References
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Polansky H, Itzkovitz E, Javaherian A. Clinical study of Gene-Eden-VIR/Novirin in genital herpes: suppressive treatment safely decreases the duration of outbreaks in both severe and mild cases. Clin Transl Med. 2016 Dec;5(1):40. doi: 10.1186/s40169-016-0121-6. Epub 2016 Oct 20.
Other Identifiers
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022015
Identifier Type: -
Identifier Source: org_study_id
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