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临床试验/NCT04720248
NCT04720248已完成不适用

Valoración Del Dolor Postoperatorio en Pacientes Sometidos a craneotomía Programada

Dr. Negrin University Hospital1 个研究点 分布在 1 个国家目标入组 73 人开始时间: 2021年2月24日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
73
试验地点
1
主要终点
Postoperative pain

研究概览

简要总结

Postoperative pain after craniotomy is frequent, with moderate-severe intensity. The fear to the side effects of opioids (nausea and vomiting and sedation), and NSAIDs (bleeding) makes it difficult to obtain adequate analgesic control in these patients. Preoperative anxiety may be associated with a poorer postoperative analgesic control, hindering the adequate postoperative evolution and increasing hospital stay and adverse effects. In this observational study, the investigators aimed to assess the postoperative analgesic management in patients undergoing scheduled craniotomy following routine clinical practice and to relate preoperative anxiety with the postoperative analgesic evaluation in this population.

详细描述

Postoperative pain after craniotomy is frequent, with moderate-severe intensity. The fear to the side effects of opioids (nausea and vomiting and sedation), and NSAIDs (bleeding) makes it difficult to obtain adequate analgesic control in these patients. On the other hand, preoperative anxiety may be associated with a poorer postoperative analgesic control and hinder the adequate postoperative evolution. The main outcome is to assess the postoperative analgesic management in patients undergoing to craniotomy. Secondary objectives are to evaluate the appearance of postoperative side effects related to the analgesics and to assess the relationship between preoperative anxiety and postoperative pain

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Patients over 18 years old undergoing scheduled form for supratentorial craniotomy.
  • Signed informed consent.

排除标准

  • Mini Mental State Examination with a score less than or equal to 24 points.
  • Patients suffering from disabilities.
  • Patients who can not collaborate in the postoperative clinical assessment.
  • Patients who can not be assessed during the postoperative period by the Acute Pain Unit.

研究组 & 干预措施

Metamizol postoperatively

Patients submitted to scheduled craniotomy receiving metamizol as analgesic medication postoperatively

干预措施: Metamizole (Drug)

结局指标

主要结局

Postoperative pain

时间窗: 48 hours postoperatively

Using the Visual Analgesic Scale (from 0 to 10, with 0 being the state corresponding to "no pain" and 10 being the "maximum pain imaginable ") and postoperative analgesic satisfaction assessed by the patient (stratified in Bad, Fair, Good or Excellent).

次要结局

  • Side effects secondary to metamizol(48 hours postoperatively)
  • To assess the correlation between preoperative anxiety and postoperative pain.(From the day before surgery to the second day postoperatively)

研究者

发起方
Dr. Negrin University Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ángel Becerra

Principal Investigator

Dr. Negrin University Hospital

研究点 (1)

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