Moi H, Morel P, Gianotti B, Barlow D, Phillips I, Jean C
Dronning Ingrids Hospital, Nuuk, Greenland.
J Antimicrob Chemother. 1996 May;37 Suppl A:115-22. doi: 10.1093/jac/37.suppl_a.115.
A double-blind, randomised, international multicentre study was conducted to compare the efficacy and safety of sparfloxacin 200 mg versus ciprofloxacin 250 mg as single oral-dose treatment for acute gonorrhoea in men. A total of 238 patients were included and 191 were evaluable for primary efficacy (eradication of Neisseria gonorrhoeae). At follow-up, 99% (96/97) of the sparfloxacin-treated patients were culture-negative compared with 98% (92/94) in the ciprofloxacin group. Three of the four patients who harboured gonococci at follow-up admitted to having had unprotected sexual intercourse after treatment and were probably reinfections. The rate of post-gonococcal urethritis was 26% in both groups, although Chlamydia trachomatis was isolated in only 4% of patients at inclusion. Both drugs were well tolerated. Single oral doses of sparfloxacin 200 mg and ciprofloxacin 250 mg are equally effective in the treatment of acute gonorrhoea in men.
开展了一项双盲、随机、国际多中心研究,以比较200毫克司帕沙星与250毫克环丙沙星单剂量口服治疗男性急性淋病的疗效和安全性。共纳入238例患者,其中191例可用于主要疗效评估(淋病奈瑟菌根除情况)。随访时,司帕沙星治疗组99%(96/97)的患者培养结果为阴性,环丙沙星组为98%(92/94)。随访时携带淋球菌的4例患者中有3例承认治疗后有未采取保护措施的性行为,可能为再次感染。两组淋菌性尿道炎的发生率均为26%,尽管纳入时仅4%的患者分离出沙眼衣原体。两种药物耐受性均良好。200毫克司帕沙星和250毫克环丙沙星单剂量口服治疗男性急性淋病疗效相当。