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临床试验/NL-OMON55905
NL-OMON55905招募中3 期

Hyperbaric OXygen therapy for ACute Acoustic Trauma - HOXACAT

Academisch Medisch Centrum0 个研究点目标入组 84 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
84

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 64(—)

入选标准

  • In order to be eligible to participate in this study, a subject must meet all
  • of the following criteria:
  • - Diagnosed with AAT based on audiometry after high impact noise-exposure at
  • the Department of Otorhinolaryngology, Central Military Hospital.
  • - First visit to the Department of Otorhinolaryngology between 24 and 72 hours
  • after the acoustic trauma.
  • - Age >= 18 years old.
  • - Minimum hearing loss: >= 30 dB on one tested frequency, or >= 25 dB on two
  • tested frequencies, OR >= 20 dB on three tested frequencies.

排除标准

  • A potential subject who meets any of the following criteria will be excluded:
  • - Subject does not speak fluent Dutch
  • - History of idiopathic sudden sensorineural loss.
  • - History of radiation therapy in the head and neck region.
  • - Previous acute acoustic trauma (before current trauma) with objectified
  • hearing loss.
  • - Current or previous use of ototoxic drugs with objectified complaints before
  • the current visit.
  • - Known presence or history of vestibular schwannoma or cholesteatoma.
  • - Current otitis media.
  • - Epilepsy.
  • - Known presence of untreated pneumothorax.
  • - Known Chronic Obstructive Pulmonary Disease Gold IV grade or other pulmonary
  • disease with severe air trapping.
  • - Known severely reduced cardiac ejection fraction.
  • - Implanted device that is not proven to be compatible with HBOT.
  • - Claustrophobia that interferes with taking place in hyperbaric chamber.
  • - Inability to equalize middle ears using Valsalva manoeuvre. (If so, patients
  • are offered tympanostomy tubes if they wish to participate before being
  • - Current pregnancy.
  • - Use of adriamycin, bleomycin, cisplatin, or doxorubicin in previous six

研究者

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