跳至主要内容
临床试验/NCT04853173
NCT04853173Unknown不适用

Modality of Pain Management in Ambulatory Tonsillectomy Surgery in Adults: External Pilot Study

Centre Hospitalier Universitaire de Besancon2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2021年5月28日最近更新:
适应症

试验速览

阶段
不适用
入组人数
30
试验地点
2
主要终点
Assess pain management modalities in ambulatory tonsillectomy surgery in adults through post-operative pain assessment, with a defined analgesia and anesthesia protocol adapted to ambulatory management.

研究概览

简要总结

No SFORL recommendation for adult ambulatory tonsillectomy. This study would allow the establishment of an ambulatory management during an adult tonsillectomy. This would allow a return home from J0 for the patient and therefore would improve the comfort of the patients and reduce the cost associated with a conventional hospitalization over several days.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
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

  • programmed Tonsillectomy surgery

排除标准

  • Congenital or acquired hemostasis disorder
  • Indication of uvulo-bike-pharyngo-plasty
  • Contraindication to the use of one of the protocol molecules including pregnancy
  • Allergy to analgesic treatments used in the study
  • Ongoing analgesic treatment that cannot be interrupted

结局指标

主要结局

Assess pain management modalities in ambulatory tonsillectomy surgery in adults through post-operative pain assessment, with a defined analgesia and anesthesia protocol adapted to ambulatory management.

时间窗: 14 days

Pain measured by self-assessment by Analog Visual Scale (0-10). If score is under 4 = efficacity of ansthesia protocol

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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