Mainguet P, Fiasse R
Gut. 1977 Jul;18(7):575-9. doi: 10.1136/gut.18.7.575.
Loperamide (R 18 553) was compared with placebo in a double-blind crossover study of 21 patients with chronic diarrhoea caused by ileocolic disease or resection. Eighteen patients completed the trial. At a median daily dose of 6 mg the new antidiarrhoeal preparation was found to be superior to placebo in controlling chronic diarrhoea. The frequency and weight of stools significantly decreased, the stools became more solid, and carmine transit time was prolonged during loperamide therapy. Loperamide was consistently preferred to placebo by the patients. Gastrointestinal side-effects were few and comparable during both treatment periods.
在一项针对21例因回结肠疾病或切除术后导致慢性腹泻患者的双盲交叉研究中,将洛哌丁胺(R 18 553)与安慰剂进行了比较。18例患者完成了试验。发现在每日中位剂量为6毫克时,这种新型止泻制剂在控制慢性腹泻方面优于安慰剂。在洛哌丁胺治疗期间,大便的频率和重量显著降低,大便变得更成形,并且胭脂红转运时间延长。患者一直更喜欢洛哌丁胺而非安慰剂。两个治疗期间的胃肠道副作用均较少且相当。