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临床试验/KCT0003439
KCT0003439尚未招募未知

Postoperative Analgesic efficacy of continuous wound INfusion after laparoscopy (PAIN): a randomized, double-blind, placebo-controlled trial

Kangbuk Samsung Medical Center0 个研究点目标入组 66 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
入组人数
66

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
18(Year) 至 65(Year)(—)
性别
Female

入选标准

  • age between 18 and 65 years,
  • - American Society of Anesthesiologists physical status (ASAPS) classification I–II,
  • - absence of pregnancy at the time of surgery

排除标准

  • - allergy to ropivacaine,
  • - laparoscopic surgery needing = 3 separate skin incisions,
  • - history of ventral or incisional hernia, pre-existing coagulopathy, neurologic or cognitive dysfunction,
  • - systemic or regional (especially, umbilicus) infection,
  • - previously taking opioids for chronic pain, or
  • - inability to accurately express their pain.

研究者

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