Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT03070314

Echinaforce Junior Bioavailability Trial

Bioavailability of an Echinacea Product (Echinaforce® Junior) in Children With a Common Cold, Aged 4-12 Years After Intake of a Daily Dosage

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
A. Vogel AG · Industry
Sex
All
Age
4 Years – 12 Years
Healthy volunteers
Not accepted

Summary

In this bioavailability trial should be shown that the one of the main active constituent in alcoholic echinacea extracts, the alkylamide dodeca-2E,4E,8Z,10E/Z-tetraenoic acid isobutylamide (short: tetraen) is bioavailable in children of different age groups after intake of 5 Echinaforce junior tablets.

Detailed description

In this bioavailability trial should be shown that the one of the main active constituent in alcoholic echinacea extracts, the alkylamide dodeca-2E,4E,8Z,10E/Z-tetraenoic acid isobutylamide (short: tetraen) is bioavailable in children of different age groups after intake of 5 Echinaforce junior tablets. Six capillary blood draws are taken at the following time points: Start (0), after 15, 30, 60, 90, 270 minutes and thereafter the bioavailability is measured and calculated.

Conditions

Interventions

TypeNameDescription
DRUGEchinaforce juniorEchinacea Purpurea Extract Pill, sweetened and with orange flavour

Timeline

Start date
2017-02-20
Primary completion
2018-06-30
Completion
2018-06-30
First posted
2017-03-03
Last updated
2018-07-18

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT03070314. Inclusion in this directory is not an endorsement.