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临床试验/NCT03218696
NCT03218696Unknown不适用

A Randomized, Double-blind Study to Evaluate the Efficacy and Tolerability of a Cough Syrup Containing Specific Plant Extracts (Poliflav M.A.) and Honey Versus Placebo in Cough Due to Upper Respiratory Tract Infection

Clalit Health Services4 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2018年2月最近更新:
适应症

试验速览

阶段
不适用
入组人数
80
试验地点
4
主要终点
Night cough frequency score reduction

研究概览

简要总结

The intent of this study is to see how boys and girls aged 1-5 and coughing since 1-2 days due to common cold respond to a specific protective cough syrup taken before going to bed for one night, with respect to a similar but not specific syrup (placebo). The symptoms evaluated include especially cough frequency but also cough intensity, bother, and sleep quality of the child and parents.

详细描述

Cough is a life saving reflex, therefore it is important, especially in pediatrics, to calm cough spells without sedating the reflex. Looking into mechanisms for cough management different from mucolytics, or sedatives, such as protection of irritated pharynx mucosa from post nasal drip or other irritating substances is theoretically sound and shows practical interesting results. A parallel comparison of efficacy and tolerability between such protective mechanism (acting through a barrier and radical scavenging action) due to natural substances (honey, plantago lanceolata and thymus vulgaris) and placebo has been looked at specifically on the clinically critical population of children coughing since 1-2 days and not more, including very young children of one year old. The intent of this study is to use the protective syrup versus placebo in children with moderate to severe night and daily cough, measured with a validated parent questionnaire. Daily cough is assessed to better describe and select the general condition of the child however only night cough parameters due to treatment are assessed. The degree of disturbance of cough is followed immediately after one night administration on all night parameters, with special interest to frequency.

Assessment of effectiveness of the protective cough syrup as compared to placebo is considered very interesting due to the mechanism of the remedy. The study looks at the effect of the syrup/placebo on the first night in order to well focus the "first" effect of a treatment on the ascending phase of the illness, such as to reduce to a minimum any interference due to natural regression of the symptom due to illness progression.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

盲法说明

According to a predertermined list, the two products are provided in identical bottles and cartons appropriately labelled so as to ensure respect of the randomization list as well as blinding of all study participants.

入排标准

年龄范围
1 Year 至 5 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Cough attributed to infection of the upper respiratory tract present in the child for not more than 2 days.
  • Children aged 1 year to 5 (ie: 1 day before the 6th birthday, males and females)
  • Score of at least 3 to two of the following three questions relating to the evaluation of night cough: frequency of nocturnal cough, impact on the sleep of the child and impact on the sleep of the parent,
  • Score of at least 3 to all three questions assessing "daytime" cough considering the day prior to study entry.
  • Written signed consent by a parent.

排除标准

  • Children with a diagnosis of acute: laryngotracheal bronchitis, pneumonia, asthma, sinusitis, allergic rhinitis, as well as chronic cardiac condition, or cystic fibrosis or any anatomical respiratory tract anomalies.
  • Children who received antihistamines or any cough medicine the day prior to study entry.
  • The administration of any steroid preparation by oral administration or inhalation on the day prior to study entry.
  • Known sensitivity to any component of placebo or to Plantago lanceolata or Thymus vulgaris, honey or any other component of the "Poliflav M.A.-honey cough syrup".

结局指标

主要结局

Night cough frequency score reduction

时间窗: First and only night of treatment

Night cough frequency is the most invasive element of distress to the child and family. The questionnaire rating night cough is filled in the morning following enrollment, relating to the passed night. The basal night score is the score of the night before enrollment.

次要结局

  • night cough intensity score reduction(First and only night of treatment)
  • night cough bothersomeness score reduction(First and only night of treatment)
  • reduction of influence of cough on parent sleep score(First and only night of treatment)
  • reduction of influence of cough on child sleep score(First and only night of treatment)
  • reduction of influence of cough on combined night score(First and only night of treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Avner Herman Cohen

Prof. Herman Avner Cohen

Clalit Health Services

研究点 (4)

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