Clinical Trials Directory

Trials / Completed

CompletedNCT01477879

Hsv 1 and 2 Gowey Protocol Versus Placebo

Phase II Clinical Trial of Versabase/Sarracenia Purpurea Versus Placebo

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
33 (actual)
Sponsor
Naturopaths International · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
OTHERVersabase gel with sarracenia purpurea 20% liquid extractTopical application of gel/plant mix to lesions
OTHERplacebo (versabase gel only)versabase gel only

Timeline

Start date
2011-01-01
Primary completion
2011-03-01
Completion
2011-03-01
First posted
2011-11-23
Last updated
2011-11-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01477879. Inclusion in this directory is not an endorsement.

Hsv 1 and 2 Gowey Protocol Versus Placebo (NCT01477879) · Clinical Trials Directory