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Effects of Echinaforce®-treatment on the response of ex vivo stimulated blood cells - Effects of Echinaforce®-treatment on ex vivo stimulated blood cells

Phase 1
Conditions
Healthy volunteers
Registration Number
EUCTR2005-004013-15-GB
Lead Sponsor
Bioforce AG
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
Not specified
Target Recruitment
24
Inclusion Criteria

Age 18-65
Healthy ie. not taking medication such as antibiotics or antiviral therapy, herbal medicine, antidepressants or have recently received vaccination
Participants who are not pregnant
Participants who are not exposed to organic solvents
Participants who have not undergone surgery within the last 3 months
Participants who do not have an allergy to plants of the compositae family
Participants who have not undertaken heavy, unusual physical activity 48 hours before first blood donation
Participants who do not have a mild stress level as assessed by PSS-10 questionnaire
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Participants who are taking medication such as antibiotics or antiviral therapy, herbal medicine, antidepressants or have recently received vaccination
Participants who are pregnant
Participants who are exposed to organic solvents
Participants who have undergone surgery within the last 3 months
Participants who have an allergy to plants of the compositae family
Participants who have undertaken heavy, unusual physical activity 48 hours before first blood donation
Participants who have a mild stress level as assessed by PSS-10 questionnaire

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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