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Study of Echinaforce Junior Tablets in Children With Acute Colds

Multicenter Open-label, Randomized Clinical Trial to Assess the Safety and Efficacy of Echinaforce® Junior Tablets in Two Dosages for the Therapy of Common Cold Symptoms in Children (4-12 Years)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02198391
Enrollment
79
Registered
2014-07-23
Start date
2014-10-15
Completion date
2015-08-07
Last updated
2021-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory Tract Diseases

Brief summary

This study aims to investigate safety and efficacy of Echinaforce Junior tablets in two dosages of 3 x 1 and 5 x 1 tablets per day in children 4 - 12 years old with acute colds.

Interventions

None listed

Sponsors

A. Vogel AG
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
4 Years to 12 Years
Healthy volunteers
Yes

Inclusion criteria

* age between 4 and 12 years * signed informed consent by parents and optionally be the child * daily access to computer / internet * competence of german language

Exclusion criteria

* 13 years or older, younger than 4 years. * presence of sinusitis, otitis media, pneumonia, bronchitis (complicated cold) at inclusion * participation in a clinical study in the past 30 days * intake of antimicrobial, antiviral, immunesuppressive substances, salicyl-containing medicines or bronchovaxom at first treatment period * surgical intervention in the 3 months before inclusion or planned intervention during the observation period * Known diabetes mellitus * Known and treated allergic rhinitis, atopy or asthma * cystic fibrosis, bronchopulmonic dysplasia, COPD * immune system disorders, degenerative diseases (e.g. autoimmune disease like AIDS or leukosis) * metabolic or resorptive disorders * liver or kidney diseases * serious health problems * predisposition for complicated cold episodes in the judgement of the physician (sinusitis, otitis media, bronchitis, pneumonia) * known allergy to plants of the compositae family (camomile or dandelion) or any of the substances of the investigational product

Design outcomes

Primary

MeasureTime frameDescription
tolerability assessment by physicians4 monthsWithin the observation period of 4 months a maximum of 3 colds can be treated with Echinaforce Junior tablets at the indicated dosage. At the exclusion visit the physicians rate the tolerability of Echinaforce Junior tablets as very good, good, moderate or bad

Secondary

MeasureTime frameDescription
tolerability assessment by parents/child4 monthsThe tolerability of Echinaforce Junior is assessed after every acute treatment period of 10 days and after the observation period of 4 months
Assessment of efficacy by parents/child4 monthsThe acute efficacy of Echinaforce Junior is rated by the parents after every acute treatment period of 10 days as well as after the observation period of 4 months
Assessment of Cold Symptoms during Acute Treatment10 daysDuring acute colds parents complete a symptom diary and assess cold-related symptoms (runny and congested nose, sneezing, headache, joint pain, sore-throat, fever, cough, shivering, sleep quality, additional care) in the child

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026