Nony P, Boissel J P, Girard P, Lion L, Haugh M C, Fareh S, De Breyne B
Unité de Pharmacologie Clinique, Hôpital Cardiologique, Lyon, France.
Fundam Clin Pharmacol. 1994;8(2):185-7. doi: 10.1111/j.1472-8206.1994.tb00796.x.
The effect of an initial single-blind placebo period in a phase I clinical trial was assessed in 12 volunteers who underwent five weekly treatment periods, consisting of treatment on the first day and a six-day wash-out period. An initial single-blind placebo period was followed by three different single doses of a platelet-aggregation factor inhibitor and another placebo period, under a double-blind Latin square design. Reports of abnormal symptoms were collected using a questionnaire designed by our group. A total of 13 abnormal symptoms were reported during the first period and only nine for the following four periods, indicating a clear placebo period effect. These preliminary results suggest that an initial single-blind period may be usefully included in phase I clinical trials.
在一项I期临床试验中,对12名志愿者进行了评估,这些志愿者经历了五个为期一周的治疗期,包括第一天的治疗和为期六天的洗脱期。在双盲拉丁方设计下,初始单盲安慰剂期之后是三种不同单剂量的血小板聚集因子抑制剂和另一个安慰剂期。使用我们小组设计的问卷收集异常症状报告。在第一个时期共报告了13种异常症状,而在随后的四个时期仅报告了9种,表明存在明显的安慰剂期效应。这些初步结果表明,初始单盲期可能有助于纳入I期临床试验。