Effectiveness of TheraNeem Lip Therapy for Herpes Simplex Labialis
Completed · Phase 1
Conditions studied: Herpes Simplex
In brief
This study intends to test the efficacy of the TheraNeem Lip Therapy balm for Herpes Simplex. The study will include a total of 5 people.
Key facts
- Study ID
- NCT00985335
- Run by
- Southern California University of Health Sciences
- People needed
- 5
- Starts
- 2009-08-01
- Expected to finish
- 2011-03-01
- Last updated by the study team
- 2011-11-18
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Participant has signs and symptoms of HSV-1 infection of less than 24 hours duration to the Southern California University of Health Sciences investigators
- Participants ages 18-70 years
- Confirmation of oral-circumoral herpes lesion will be made by a clinician in the presence of oral-circumoral lesion assumed to be HSV-1 for purposes of study
- Subjects expressed willingness to comply with protocol
- Subject will be willing to have the presenting lesion photographed twice
- Subject sign a written informed consent, HIPPA disclosure, Experimental bill of rights
You may not qualify if…
- History of past or present immunosuppressive condition, or currently taking immunosuppressive medication
- History of adverse effects or allergies to any Neem based product or containing any of the other ingredients TheraNeem Lip Therapy: Organic Coconut Oil, Organic Beeswax, Organic Jojoba Oil, Shea Butter, Sesame Oil, Organic Neem Oil, , Essential Oil of Peppermint, Vitamin E (Tocopherol)
- Signs of disseminated HSV illness
- History of use of oral or topical antiviral agents within 10 days of screening and/or at start of study visit
- Pregnancy or lactation
- Psychiatric disorder
- Inability to understand or follow the instructions
Where it is running
- Southern California University of Health Science — Whittier, California, United States
Full record on ClinicalTrials.gov
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