跳至主要内容
临床试验/NCT06374849
NCT06374849进行中(未招募)4 期

Intraoperative Sufentanil and Chronic Postsurgical Pain in Non-major Scheduled Abdominal Surgery

Centre Hospitalier Universitaire, Amiens2 个研究点 分布在 1 个国家目标入组 855 人开始时间: 2024年6月24日最近更新:
适应症

试验速览

阶段
4 期
状态
进行中(未招募)
入组人数
855
试验地点
2
主要终点
Incidence of CPSP

研究概览

简要总结

Several risk factors for chronic postoperative pain have been identified. A series of studies have shown that administrating intraoperatively a high dose of Remifentanil is associated with an increased incidence of CPSP. These findings highlight a risk factor for CPSP that the anaesthetist can influence on, but they however remain limited to remifentanil. To this day, no study have attempted to evaluate the existence of such an association between the incidence of CPSP and the intraoperative administration of sufentanil doses. Improved knowledge of the long-term nociceptive impact of intraoperative sufentanil administration would enable better therapeutic adaptation according to each patient's risk.

In the field of CPSP, non-major abdominal surgeries remain poorly studied. This is due to their lower risk of CPSP than other surgeries such as orthopaedic, mammary or thoracic surgery. Nevertheless, they constitute a large number of daily surgical procedures. The estimated incidence of CPSP in non-major abdominal surgery appears in several studies to be between 15 and 20% The aim of this study is to evaluate the correlation between the intraoperative administration of sufentanil doses and the incidence of CPSP at 3 months in patients undergoing non-major scheduled abdominal surgery.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age > 18 years old.
  • Non-major scheduled abdominal surgery.
  • Patient will receive Sufentanil intraoperatively for induction and maintenance of general anesthesia
  • 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.
  • Pregnancy.
  • Ambulatory surgery.
  • Endoscopic surgery.
  • Surgery with loco-regional or perimedullary anesthesia without general anesthesia
  • Intraoperative use of an opioid other than Sufentanil.
  • Hypersensitivity to sufentanil
  • Legally protected patients (under judicial protection, guardianship, curatorship).
  • 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…)

结局指标

主要结局

Incidence of CPSP

时间窗: at 3 months

Incidence of CPSP at 3 months after non-major scheduled abdominal surgery

次要结局

  • Post-operative pain intensity(at 48 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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