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临床试验/TCTR20210922004
TCTR20210922004Unknown1 期

a comparison of patient satisfaction among topical anesthetic techniques in transnasal fiberoptic laryngoscopy, A double-blinded randomized controlled trial

faculty of medicine, Khon Kaen University0 个研究点目标入组 210 人开始时间: 2021年9月22日最近更新:
适应症

试验速览

阶段
1 期
入组人数
210

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 Years 至 60 Years(—)
性别
All

入选标准

  • 1. age 18-60 years
  • 2. this is the first time the patient undergoing transnasal fiberoptic laryngoscopy
  • 3. patient can read-write in Thai

排除标准

  • 1. patients who can not tell their pain score
  • 2. patients who have been used transnasal topical anesthesia before
  • 3. patients who are allergic to Amide-group drug
  • 4. patients who have hemodynamic instability
  • 5. patients who are at risk for upper airway obstruction
  • 6. patients who have any pathology in nose that fiberoptic laryngoscopy can not pass
  • 7. patients who suspected from having any pathology in nose
  • 8. patients who have tracheostomy
  • 9. patients who have cerebrovascular disease that might have sensory deficit
  • 10. patients whom the procedure need to pass true vocal cord

研究者

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