Expired Study
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St. Petersburg, Florida 33710


Purpose:

This study will evaluate the primary irritation potential of NatrOVA Creme Rinse - 1% in humans, after exposure to UV radiation.


Criteria:

Inclusion Criteria: 1. Male or female subjects 18-65 years of age and in good health. 2. Fitzpatrick skin type I, II or III Exclusion Criteria: 1. History of severe reactions from exposure to sunlight 2. Known allergies or sensitivities to adhesives in patches 3. Inability to evaluate the skin in and around the test sites 4. Diabetes requiring medication 5. Clinical significant skin disease 6. Asthma or other severe respiratory disease 7. Known immunological disorders such as HIV, AIDS, lupus,rheumatoid arthritis 8. History or current skin cancer 9. Mastectomy for cancer involving removal of lymph nodes draining the test sites 10. Epilepsy 11. Pregnancy, lactation, or planned pregnancy during study period 12. Chronic use of systemic antihistamine medication within 14 days of screening 13. Use of anti-inflammatory drugs within 2 days of Screening Visit 1 14. Currently receiving allergy injections 15. Use of immunosuppressive drugs 16. Topical drugs used at the test site within 7 days of Screening Visit 1 17. Current participation in any clinical trial 18. Participation in any patch test for irritation or sensitization or UV exposures within 4 weeks of study start 19. Use of any investigational drug therapy within 4 weeks of study start.


NCT ID:

NCT00591331


Primary Contact:

Principal Investigator
John V Murray, MD
Hill Top Research


Backup Contact:

N/A


Location Contact:

St. Petersburg, Florida 33710
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: June 25, 2018

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