跳至主要内容
临床试验/NCT05916768
NCT05916768已完成不适用

Management of Acute Bronchitis in Switzerland With Pelargonium Sidoides Extract EPs®7630 Versus Usual Care - a Pragmatic, Open-label, Randomised Controlled Trial

University of Fribourg1 个研究点 分布在 1 个国家目标入组 332 人开始时间: 2023年5月15日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
332
试验地点
1
主要终点
Effectiveness of Pelargonium sidoides extract EPs® 7630

研究概览

简要总结

The aim of our study is to conduct a pragmatic RCT meeting all required standards to evaluate the effectiveness of Pelargonium sidoides extract, EPs® 7630, in the management of acute bronchitis with or without COVID-19 in PCP practices and walk-in clinics in French-speaking Switzerland. The RCT will be preceded by a pilot phase to ensure its feasibility.

详细描述

The goal of this clinical trial is to evaluate the effectiveness of Pelargonium sidoides extract EPs® 7630, also known under the brand name Kaloba®, in the management of acute bronchitis.

The main questions it aims to answer are:

  • Is Pelargonium sidoides extract EPs® 7630 effective to reduce the severity and the duration of symptoms related to acute bronchitis ?
  • Does Pelargonium sidoides extract EPs® 7630 allow to reduce the prescription of antibiotics?

Participants will be randomize 1:1 either in the control group (usual care) or in the intervention group (Pelargonium sidoides extract EPs® 7630).

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
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

  • Adult patients (aged 18 and over) consulting for the first time, for the same episode, either for an acute cough (≤8 days) as the main symptom, suggestive of acute bronchitis, or for an illness (≤8 days) in which cough is not the main symptom but PCP believes that acute bronchitis is the most likely diagnosis.
  • Patients tested positive to COVID-19 who meet the above-mentioned criteria will be included too.

排除标准

  • Infection requiring antibiotic treatment (ex. cystic fibrosis)
  • Pneumonia
  • Known hypersensitivity to Pelargonium sidoides extract or excipients of the trial medication
  • Non-infectious causes (COPD, asthma, pulmonary embolism, heart failure, gastroesophageal reflux, allergy)
  • Lacking the faculty of discernment (for example: dementia, decompensated psychosis or severe depression)
  • Inability to fill out the diary (no ability to read and understand French)
  • Pregnancy or breastfeeding
  • Immunological deficiencies
  • Hospitalization
  • Severe hepatic disease
  • Patients who have already started a treatment with Pelargonium sidoides EPs® 7630 for this current episode (Kaloba®, Umckaloabo®)
  • Important risk of bleeding (severe thrombocytopenia and anticoagulant intake)
  • If the patient is taking a drug among these classes of drugs:
  • anticoagulants, immunosuppressants, chemotherapy or immunotherapy

结局指标

主要结局

Effectiveness of Pelargonium sidoides extract EPs® 7630

时间窗: 22 days

Effectiveness will be determined by comparing the number of days needed to achieve a 50% reduction in the ABSS score after peak of symptoms in each group.

Proportion of patients taking antibiotics

时间窗: 22 days

The co-medication, including antibiotics, will be collected by the investigator at day 4, 8 and 22. The results will be compared between the two arms.

次要结局

  • Integration of a herbal medicinal product in conventional settings(22 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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