跳至主要内容
临床试验/CTIS2023-510140-21-00
CTIS2023-510140-21-00进行中(未招募)1 期

Intraoperative Sufentanil and chronic postsurgical pain in non-major scheduled abdominal surgery - PI2023_843_0173

Centre Hospitalier Universitaire Amiens Picardie0 个研究点目标入组 855 人开始时间: 2023年12月18日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
855

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Age > 18 years old, Non-major scheduled abdominal surgery., Written or oral informed consent to participate in the study.

排除标准

  • Intraoperative complications that are life-threatening or require the surgical procedure to be discontinued, Repeat surgery at the same surgical site in less than 3 months, Ambulatory surgery and Endoscopic surgery, Surgery with loco-regional or perimedullary anesthesia without general anesthesia, Intraoperative use of an opioid other than Sufentanil, Patients suffering from psychiatric pathologies, Patients suffering from neurodegenerative pathologies, Patients for whom self-assessment of pain using an numerical rating scale (0-10) is not feasible (language barrier, etc…)

研究者

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