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临床试验/NL-OMON43878
NL-OMON43878已完成不适用

Deep and slow breathing in postsurgical abdominal pain management: an explorative study - Deep breathing after major abdominal surgery

Radboud Universitair Medisch Centrum0 个研究点目标入组 40 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
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • 1.Patient is at least 18 years old on the day the informed consent form will be signed.
  • 2.Patient is undergoing elective major abdominal surgery.
  • 3.The surgical procedure has an estimated duration of at least 90 minutes, excluding the time to induce anesthesia.
  • 4.Patient scores I to III in the American Society of Anesthesiologists physical status classification system (ASA I-III).
  • 5.Patient is willing and able to comply with the trial protocol.
  • 6.Patient is able to speak, read and understand the local language of the investigational site, is familiar with the procedures of the study, and agrees to participate in the study program by giving oral and written informed consent.

排除标准

  • 1. Severe chronic obstructive or another pulmonary disease that impairs patient from practicing deep and slow breathing
  • 2.Patient has (a history of) a (chronic) pain syndrome that interferes with the interpretation of QST results.
  • 3.Patient has (a history of) Raynaud syndrome or fenomenon, or a medical disorder that interferes with the study measurements or may pose a risk for the patient.
  • 4.Patient does not feel a pinprick test to the lower extremities, due to affected sensory input (e.g. neuropathy as a result of diabetes mellitus).
  • 5.Female patient is pregnant during the course of the study.
  • 6.Patient is allergic to white plasters.
  • 7. Any condition that disables the patient to make an independent transfer from bed to chair, e.g. being wheelchair bound.

研究者

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