Herpes Simplex Virus-1: A Pilot Study Using Hand Sanitizer

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Early Phase 1
SUMMARY

The purpose of this pilot study is to determine if the use of Purell hand sanitizer alters the duration, level of pain and discomfort during treatment, and the size of the HSV-1 lesion. The duration of an HSV-1 (herpes) lesion is the primary endpoint for this study. Size, pain, and discomfort are the secondary endpoints.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: t
View:

⁃ For the purpose of this study participants must be:

• in the early prodromal stage of an HSV-1 outbreak (less than 24 hours from initial symptom)

• have a visible manifestation of a lesion

• be 18 years or older

• capable of following daily treatment instructions

• willing to complete a daily journal

• willing to come to the clinic twice for records and pictures during the14 days that the lesion is present or until participant is free of lesion.

Locations
United States
Idaho
Idaho State University
RECRUITING
Pocatello
Utah
Cotton Creek Dental
RECRUITING
St. George
Utah Tech University
RECRUITING
St. George
Contact Information
Primary
Leciel Bono, MS
bonoleci@isu.edu
2082823076
Backup
Amanda Gibbs, MS candidate
amandagibbs@isu.edu
(801)450-3509
Time Frame
Start Date: 2022-04-08
Estimated Completion Date: 2023-11-30
Participants
Target number of participants: 20
Treatments
Experimental: Treatment Group (Hand Sanitizer)
Participants with an early prodromal stage of an HSV-1 outbreak (less than 24 hours from initial symptom), with the visible manifestation of a lesion will be invited to participate in the study. Participants will apply a large drop of hand sanitizer in an unmarked container to a Q-tip and will hold the Q-tip on the lesion for 10 seconds. The hand sanitizer will be administered every waking hour in the same manner.
Placebo_comparator: Control Group (Medical Grade Mineral Oil)
Participants with an early prodromal stage of an HSV-1 outbreak (less than 24 hours from initial symptom), with the visible manifestation of a lesion will be invited to participate in the study. Participants will apply a large drop of Medical Grade Mineral Oil in an unmarked container to a Q-tip and will hold the Q-tip on the HSV-1 lesion for 10 seconds. The medical grade mineral oil will be administered every waking hour in the same manner.
Related Therapeutic Areas
Sponsors
Leads: Leciel Bono

This content was sourced from clinicaltrials.gov

Similar Clinical Trials