首页> 外文期刊>International journal of clinical oncology >Efficacy and safety of sublingual fentanyl orally disintegrating tablet at doses determined by titration for the treatment of breakthrough pain in Japanese cancer patients: a multicenter, randomized, placebo-controlled, double-blind phase III trial
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Efficacy and safety of sublingual fentanyl orally disintegrating tablet at doses determined by titration for the treatment of breakthrough pain in Japanese cancer patients: a multicenter, randomized, placebo-controlled, double-blind phase III trial

机译:滴定剂量的舌下芬太尼口腔崩解片治疗日本癌症患者突破性疼痛的疗效和安全性:一项多中心,随机,安慰剂对照,双盲III期临床试验

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摘要

Background Breakthrough cancer pain typically has a rapid onset and relatively short duration. Due to this temporal profile, it may not be adequately relieved by oral opioid analgesics. The sublingual fentanyl orally disintegrating tablet is a formulation by which fentanyl can be rapidly absorbed across the oral mucosa producing rapid-onset analgesia, and which may be effective for breakthrough pain treatment.
机译:背景技术突破性癌症疼痛通常起效快且持续时间相对较短。由于这种时间特性,口服阿片类镇痛药可能无法充分缓解。舌下芬太尼口腔崩解片是一种制剂,通过该制剂,芬太尼可以在口腔粘膜上迅速吸收,从而产生快速起效的镇痛作用,并且可能对突破性疼痛治疗有效。

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