Fourteen-day safety and acceptability study of 6% cellulose sulfate gel: a randomized double-blind Phase I safety study

被引:75
作者
Schwartz, Jill L. [1 ]
Mauck, Christine
Lai, Jaim-Jou
Creinin, Mitchell D.
Brache, Vivian
Ballagh, Susan A.
Weiner, Debra H.
Hillier, Sharon L.
Fichorova, Raina N.
Callahan, Marianne
机构
[1] Eastern Virginia Med Sch, CONRAD, Dept Obstet & Gynecol, Arlington, VA 22209 USA
[2] Family Hlth Int, Res Triangle Pk, NC 27709 USA
[3] Univ Pittsburgh, Dept Obstet Gynecol & Reprod Sci, Pittsburgh, PA 15213 USA
[4] Magee Womens Res Inst, Pittsburgh, PA 15213 USA
[5] Profamilia, Santo Domingo 10401, Dominican Rep
[6] Eastern Virginia Med Sch, CONRAD, Dept Obstet & Gynecol, Norfolk, VA 23507 USA
[7] Brigham & Womens Hosp, Dept Obstet Gynecol & Reprod Biol, Boston, MA 02120 USA
[8] Harvard Univ, Sch Med, Boston, MA 02120 USA
关键词
cellulose sulfate; contraception; microbicide; sexually transmitted infection; clinical trial;
D O I
10.1016/j.contraception.2006.02.008
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Background: Topical microbicides against the human immunodeficiency virus (HIV) 1 that are nonirritating to the female genital epithelium are urgently needed to slow the heterosexual spread of HIV infection. Products that are also effective contraceptives provide additional benefits. Cellulose sulfate (CS) is a noncytotoxic antifertility agent that exhibits in vitro antimicrobial activity against sexually transmitted pathogens, including HIV. Methods: We performed a multicenter, Phase I, placebo-controlled, randomized study to evaluate the genital toxicity of CS. Two cohorts of healthy women used 3.5 ml of 6% CS gel or 3.5 ml of K-Y Jelly, vaginally, bid, for 14 days. The first cohort was sexually abstinent, and the second cohort was sexually active. Results: CS was associated with only a slightly higher odds ratio (OR) of symptoms of minor urogenital irritation compared to the inactive lubricant K-Y Jelly (OR 2.02, 95% confidence interval = 0.90-4.53). In addition, there were minor shifts in some genital flora, but there was no evidence of greater inflammation as evidenced by few colposcopic findings, decreased influx of polymorphonuclear cells and minimal changes in proinflammatory cytokines. Moreover, both products appeared acceptable to most women. Product leakage was identified as more of a problem in sexually abstinent women, but less so in women using the product for sexual intercourse, as would be the case in actual practice. Conclusion: CS was safe for twice-daily use for 14 days. CS is appropriate for future studies in effectiveness trials. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:133 / 140
页数:8
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