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临床试验/NCT00611390
NCT00611390已完成1 期

Treatment of Acute Tracheitis and Laryngitis With Essential Oils of Some Aromatic Medical Plants.

HaEmek Medical Center, Israel2 个研究点 分布在 1 个国家目标入组 29 人开始时间: 2008年1月最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
29
试验地点
2
主要终点
To demonstrate a cough or hoarseness relief within the first 20 minutes after first administration of treatment with the spray.

研究概览

简要总结

This randomized, double blind, parallel group study, compared the efficacy of spray containing aromatic essential oils of some herbal plants, against placebo in the treatment of patients with acute viral Laryngitis or Tracheitis.

Study objectives: Primary to demonstrate a hoarseness or cough relief within 20 minutes after first administration of treatment with the spray.

Secondary to demonstrate a reduction of a defined symptoms sum score based on symptoms and signs comparing baseline therapy from the beginning to the end of 3 days treatment

详细描述

This study compared the efficacy of spray containing aromatic essential oils of Eucalyptus citriodora, Eucalyptus globulus, Mentha piperita, Origanum syriacum, and Rosmarinus Officinalis, against placebo in the treatment of patients with acute viral Laryngitis or Tracheitis.

In- vitro and clinical studies suggest therapeutic potential of aromatic herbs and trees oils in the treatment of Laryngitis or Tracheitis. The pharmacological and clinical activity of Eucalyptus citriodora, Eucalyptus globulus, Mentha piperita, Origanum syriacum, and Rosmarinus Officinalis, include anti-inflammatory, anti-bacterial and anti-viral activities. Some of these herbs and trees oils have direct activity on the respiratory tract, the coughing reflex and the airflow in the nasal tract.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

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

  • Clinical diagnosis of acute viral Laryngitis or viral tracheitis.
  • Active disease less than 48 hours
  • Patients agree to sign informed consent according to GCP and Israel national regulations.

排除标准

  • Acute lower respiratory tract infection.
  • C.O.P.D.(Chronic Obstructive Pulmonary Disease)
  • Under any antibiotically treatment.
  • Asthma disease.
  • Under coumadine therapy.
  • Hyper sensitivity to Aromatic essential oils.
  • Any immuno-suppressive disease

结局指标

主要结局

To demonstrate a cough or hoarseness relief within the first 20 minutes after first administration of treatment with the spray.

时间窗: 20 minutes

次要结局

  • To demonstrate a reduction of a defined symptoms sum score based on symptoms and signs comparing baseline therapy from the beginning to the end of 3 days treatment.(3 days)

研究者

申办方类型
Other

研究点 (2)

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