Abstract |
A double-blind, placebo-controlled study was done to evaluate the efficacy of an alpha interferon preparation in 128 patients with recurrent genital herpes. The preparation containing 10(5) or 10(7) U alpha interferon with nonoxynol 9 in a cream base (Exovir-HZ) was applied three times daily for 5 days. The treatment did not cause any adverse reactions. Patients treated with either interferon concentration became negative for viral culture at a faster rate than placebo recipients. The end of new lesion formation, scabbing, and the healing of lesions were all superior in patients treated with 10(5) U to those treated with 10(7) U interferon. End of new lesion formation and scabbing were also statistically different in patients treated with 10(7) U from those patients treated with placebo. Results suggest that topical interferon might be useful in relieving symptoms of severe cases of genital herpes.
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Authors | A E Friedman-Kien, R J Klein, R D Glaser, S M Czelusniak |
Journal | Journal of the American Academy of Dermatology
(J Am Acad Dermatol)
Vol. 15
Issue 5 Pt 1
Pg. 989-94
(Nov 1986)
ISSN: 0190-9622 [Print] United States |
PMID | 3023457
(Publication Type: Clinical Trial, Controlled Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Drug Combinations
- Gels
- Interferon Type I
- Nonoxynol
- Polyethylene Glycols
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Topics |
- Administration, Topical
- Clinical Trials as Topic
- Double-Blind Method
- Drug Combinations
- Female
- Gels
- Herpes Genitalis
(drug therapy)
- Humans
- Interferon Type I
(administration & dosage, therapeutic use)
- Male
- Nonoxynol
- Polyethylene Glycols
(administration & dosage, therapeutic use)
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