編盲是藥物臨床試驗(yàn)的重要環(huán)節(jié)，可直接影響到臨床試驗(yàn)盲法實(shí)施的質(zhì)量。目前編盲工作存在的問題有參與各方責(zé)任明確，但監(jiān)管尚有不及；參與人員的實(shí)際工作經(jīng)驗(yàn)不足，缺乏系統(tǒng)培訓(xùn)；安慰劑制備質(zhì)量參差不齊，存在較大破盲風(fēng)險；編盲現(xiàn)場操作不規(guī)范，對編盲現(xiàn)場工作流程及細(xì)節(jié)不能充分把握，嚴(yán)重影響工作的質(zhì)量和效率?；诰幟すぷ髦写嬖诘膶?shí)際問題，提出具體建議：明確監(jiān)管方，提高監(jiān)管力度；強(qiáng)化責(zé)任意識，重視責(zé)任歸屬；明確人員分工，加強(qiáng)規(guī)范培訓(xùn)；適應(yīng)工作需求，不斷完善標(biāo)準(zhǔn)操作規(guī)程（SOP）。以期與同行探討，共同推動編盲工作的標(biāo)準(zhǔn)化與規(guī)范化，從源頭為臨床試驗(yàn)盲法的開展奠定堅(jiān)實(shí)的基礎(chǔ)。

Blinding is an important segment of drug clinical trials, which can directly affect the quality of clinical trial. The current problems of blinding are as follows: Responsibilities clearly of all participants but lack of supervision; due to lack of training, there is a significant difference in the abilities and experiences of the participants. There is a high risk of blinding failure cause of the quality of placebo preparation varies. The on-site operation of blinding is not standardized, which seriously affects the quality and efficiency of work. Based on the above issues, suggestions include: Clarifying regulatory authorities and increasing regulatory efforts, strengthening the sense of responsibility and attaching importance to the attribution of responsibility, clarifing personnel division of labor and strengthening standardized training, improving standard operating procedures (SOP) continuously in order to adapt working needs. The standardization process of the blinding requires peer communication. Supervision and responsibility are important guarantees for the high-quality blinding implementation in clinical trials.

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重大新藥創(chuàng)制科技重大專項(xiàng)（2017ZX09304019）；北京中醫(yī)藥大學(xué)東直門醫(yī)院 2022 科技創(chuàng)新專項(xiàng)（DZMKJCX-2022-013）