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临床试验/NL-OMON47724
NL-OMON47724已完成不适用

Elective Umbilical Hernia Repair: Outcomes of postoperative Pain in Adults after local Wound Infiltration or ultrasound-guided bilateral REctus Sheath block. (EUHROPA WIRES trial) - EUHROPA WIRES trial

Maxima Medisch Centrum0 个研究点目标入组 66 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
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

入排标准

年龄范围
18 至 99(—)

入选标准

  • Adult (*18 years old) patients with an ASA-classification between I-III, who are planned for primary elective umbilical hernia repair.

排除标准

  • - Patients undergoing primary EUHR via scopic surgical technique.
  • - Patients undergoing emergency umbilical hernia repair or patients with any previous history of umbilical hernia repair.
  • - Patients with simultaneous repair of other hernia defects or other surgical procedures performed during the primary EUHR.
  • - Patients with an ASA-classification >III.
  • - Patients with any contraindications for an USBRSB or LWI.
  • - Known allergies for LA drugs, or allergies for LA drugs that become apparent during the study course.
  • - Patients under chronic treatment with analgesic drugs or patients with any previous history with the medical subspecialty of Pain Medicine.
  • - Patients with any previous history of a laparotomy or stoma.
  • - Patients without informed consent (IC) and patients without the mental capacity for self-determination.

研究者

发起方
Maxima Medisch Centrum

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