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Hsv 1 and 2 Gowey Protocol Versus Placebo

N

Naturopaths International

Status and phase

Completed
Phase 2
Phase 1

Conditions

Herpes

Treatments

Other: placebo (versabase gel only)
Other: Versabase gel with sarracenia purpurea 20% liquid extract

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This study will compare efficacy of versabase gel with 20% sarracenia purpurea versus placebo applied every 3-4 hours to herpes lesions.

Full description

Patients screened for hsv one or two. Patients with herpes given a 1/8 oz of gel. Researcher does not know which is active and which is placebo (placebo is actually just versabase gel). Patent applies gel to lesions every 3-4 hours. Returns to clinic on days 3, 5, and 14 for evaluation. Up to 50 patients may be enrolled.

Enrollment

33 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Hsv 1&2

Exclusion criteria

  • No active lesions

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Quadruple Blind

33 participants in 2 patient groups, including a placebo group

Versabase/20% S. purpurea extract
Active Comparator group
Treatment:
Other: Versabase gel with sarracenia purpurea 20% liquid extract
placebo (versabase gel only)
Placebo Comparator group
Description:
placebo used will be versabase gel alone
Treatment:
Other: placebo (versabase gel only)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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