MedPath

Superiority of Newly Developed Over Basic Echinacea Formulations for the Treatment of Respiratory Tract Infections

Phase 2
Completed
Conditions
Respiratory Tract Infections
Interventions
Registration Number
NCT03812900
Lead Sponsor
A. Vogel AG
Brief Summary

This is a comparative, conceptual, randomized clinical study to investigate newly developed over basic Echinacea formulations for the treatment of acute symptoms of respiratory tract infections. 400 adults will be recruited, of which approximately 300 will develop a common cold or a influenza-like infection. Two newly developed and two existing Echinacea formulations (solid/liquid) will be randomly dispensed at inclusion for treatment of maximal 3 infections. Treatment starts at first signs of infection and lasts for a maximum of 10 days or until symptom resolution. Nasopharynx samples will be collected for analysis of common viral respiratory agents throughout treatment. Safety and efficacy variables will be assessed.

Detailed Description

The monocentre trial compares two newly developed pharmaceutical forms of Echinacea (extract from Echinacea purpurea Herba and Radix; lozenges or spray) with two basic and authorised pharmaceutical forms (tablets or drops; comparator groups) for the treatment of acute symptoms of the common cold and/or influenza-like illness (ILI) in adults. Trial subjects are preventatively screened and included in the study (n = 400). If they show acute symptoms of a common cold or ILI during the study period, they are instructed to call the study centre to have confirmed the indication for treatment and begin with the treatment, they are randomized to (1:1:1:1 randomization into one of four groups). The primary endpoint is the time until remission of respiratory symptoms with the new pharmaceutical forms compared to the basic forms during the first episode. Secondary endpoints include remission of all treated episodes (max. 3 episodes), remission times comparison between different pharmaceutical forms (e.g. lozenges vs. spray, lozenges vs. drops etc), reduction of viral load on day 5 and 9 compared to day 1 of treatment (nasopharyngeal swabs), differences in safety (blood parameters before and during treatment), differences in number of adverse events, tolerance and efficacy assessed by the patients.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
246
Inclusion Criteria
  • At least 18 years old
  • Signed Informed Consent
Exclusion Criteria
  • Younger than 18 years
  • Participation in another clinical study in the past 30 days
  • Permanent intake of antimicrobial, antiviral, immune suppressive substances
  • Surgical intervention in the 3 months prior to inclusion or planned surgery during period of observation
  • Known diabetes melitus
  • Known and treated atopy or asthma bronchiale
  • Cystic fibrosis, bronchopulmonale dysplasia, COPD
  • Known diseases of the immune system, degenerative illnesses (e.g. auto-immune disorders like AIDS or leukemia, myeloma)
  • Known metabolic or resorptive disorders
  • Known chronic liver diseases (chronic hepatitis, liver cirrhosis)
  • Known chronic kidney insufficiency
  • Serious health issues (reduced health status, autoimmune illness, tumorous illness)
  • Known allergy to plants of compositae family (camomille, dandelion) or to any substances of the investigational product
  • At inclusion known pregnancy or planned pregnancy during period of investigation (required: active contraception for women of childbearing year)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Formulation DEchinacea purpurea alcoholic extractEchinacea purpurea alcoholic extract, drops (basic formulation, reference)
Formulation AEchinacea purpurea alcoholic extractEchinacea purpurea alcoholic extract lozenges (novel formulation)
Formulation BEchinacea purpurea alcoholic extractEchinacea purpurea alcoholic extract spray (novel formulation)
Formulation CEchinacea purpurea alcoholic extractEchinacea purpurea alcoholic extract tablet (basic formulation, reference)
Primary Outcome Measures
NameTimeMethod
Time to remission from initial episodesmaximally 10 days

duration until respiratory symptoms are solved

Secondary Outcome Measures
NameTimeMethod
Time to remission from overall episodesmaximally 10 days

duration until respiratory symptoms are solved

Blood safety (red and white cell count)At Inclusion visit and day 5 of infection

Change of blood parameters before (V1) and after treatment (V2)

Blood safety (creatinin [umol/l])At Inclusion visit and day 5 of infection

Change of blood parameters before (V1) and after treatment (V2)

Blood safety (ALT [ukat/l])At Inclusion visit and day 5 of infection

Change of blood parameters before (V1) and after treatment (V2)

Blood safety (AST [ukat/l])At Inclusion visit and day 5 of infection

Change of blood parameters before (V1) and after treatment (V2)

Cross-comparison of remissions between formulationsmaximally 10 days

duration until respiratory symptoms are solved

Development of single respiratory symptomsmaximally 10 days

Comparison of respiratory symptom scores between formulations, adapted Jackson Score \[0-3, 0=absent, 3=severe\]

Development of respiratory symptom sum scoremaximally 10 days

Comparison of symptom sum scores between formulations, adapted Jackson Score \[0-27, each 0=absent, 3=severe\]

Absence from School/Workduring acute respiratory episodes, 7 days each

Number of days absent from work or school

Reduction of viral load in nasopharyngeal samplesday 1, day 5, day 9

Comparison of virus titer at day 5 and 9 i.c. to day 1

Subjective assessment of efficacy by patientAt end of treatment cycle of 10 days

Comparisons of subjective efficacy assessments between patients \[0=poor; 1=moderate; 2=good; 3=very good\]. Inofficial scale and and global method of assessing patients satisfaction re efficacy.

Blood safety (Bilirubin [umol/l])At Inclusion visit and day 5 of infection

Change of blood parameters before (V1) and after treatment (V2)

Acceptance of treatmentAt end of treatment cycle of 10 days

Question:"would you use the medicament again?"

Concomitant medication and -therapyduring acute respiratory episodes of 10 days

Incidence of concomitant medication and -therapy

adverse eventsduring acute respiratory episodes, from day 1 until follow up at day 17 - 21

occurrence of adverse events during treatment with Echinacea

Subjective assessment of tolerability by patientAt day 10 of every treatment cycle

Comparisons of subjective tolerability assessments between patients \[0=poor; 1=moderate; 2=good; 3=very good\]. Inofficial scale and and global method of assessing patients satisfaction re tolerability.

Trial Locations

Locations (1)

Cantonal Hospital St. Gallen

šŸ‡ØšŸ‡­

Saint Gallen, Switzerland

Ā© Copyright 2025. All Rights Reserved by MedPath