Stolz E, Wagenvoort J H, van der Willigen A H
Department of Dermatology and Venereology, Rotterdam, The Netherlands.
Pharm Weekbl Sci. 1987 Dec 11;9 Suppl:S82-6. doi: 10.1007/BF02075269.
The results of two therapeutic trials in female patients with uncomplicated urogenital gonorrhoea (A) and in male patients with uncomplicated urethral gonorrhoea (B) treated with either 200 mg and 400 mg enoxacin orally, of one therapeutic trial in male patients with uncomplicated urogenital gonorrhoea treated with either 250 mg or 500 mg ciprofloxacin orally (C) and of one therapeutic trial in male patients with non-gonococcal urethritis (NGU) treated with ciprofloxacin 1 g daily during seven days (D) are presented and compared with the results of other investigators. The cure rate in study A was 100% (n = 40) in the 400 mg group and 95.7% (n = 46) in the 200 mg group. The cure rate in study B was 92% (n = 78) in the 400 mg group and 90% (n = 77) in the 200 mg group. In both studies no antichlamydial effect of enoxacin was observed. The cure rates in study C were 100% with 250 and 500 mg. An antichlamydial effect seemed to be present. In studies A, B and C side effects were minor and rare and were mainly nausea and headache. In study D (100 patients suffering from NGU) disappearance of Chlamydia trachomatis and Ureaplasma urealyticum one day after the end of treatment was observed in 29 of 32 (91%) and 28 of 32 (88%) cases, respectively. Pyuria disappeared in 44% and 74% of the patients showed clinical cure. However, two weeks after the end of treatment Chlamydia trachomatis and Ureaplasma urealyticum were observed in respectively six and eight cases. In 30% pyuria was still absent. Side effects were only minor.(ABSTRACT TRUNCATED AT 250 WORDS)
本文展示了两项治疗试验的结果,并与其他研究者的结果进行了比较。试验A为口服200毫克和400毫克依诺沙星治疗女性单纯性泌尿生殖系统淋病患者,试验B为口服同样剂量依诺沙星治疗男性单纯性尿道炎患者,试验C为口服250毫克或500毫克环丙沙星治疗男性单纯性泌尿生殖系统淋病患者,试验D为口服环丙沙星1克,连续7天治疗男性非淋菌性尿道炎(NGU)患者。试验A中,400毫克组治愈率为100%(n = 40),200毫克组为95.7%(n = 46)。试验B中,400毫克组治愈率为92%(n = 78),200毫克组为90%(n = 77)。两项试验均未观察到依诺沙星的抗衣原体作用。试验C中,250毫克和500毫克组治愈率均为100%,似乎存在抗衣原体作用。试验A、B和C中副作用轻微且罕见,主要为恶心和头痛。试验D(100例NGU患者)中,治疗结束一天后,32例中有29例(91%)沙眼衣原体消失,32例中有28例(88%)解脲脲原体消失。脓尿消失率为44%,74%的患者临床治愈。然而,治疗结束两周后,分别有6例和8例患者仍检测到沙眼衣原体和解脲脲原体。30%的患者仍无脓尿。副作用仅为轻微。(摘要截选至250字)