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Effects of Echinacea in Children

Assessing the in Vivo Effect of Echinacea Purpurea on Markers of Immune Activities in Children

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00773435
Enrollment
0
Registered
2008-10-16
Start date
2008-11-30
Completion date
2009-08-31
Last updated
2015-12-02

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

Conditions

Upper Respiratory Infections

Keywords

Upper respiratory tract infections, Children, Echinacea, Prevention, Immune modulation

Brief summary

The goal of the this study is to determine if Echinacea purpurea stimulates the immune system in children. For the study, 40 healthy children, 6-11 years old will be randomized to receive Echinacea purpurea or placebo for 10 days in 3 consecutive months. Blood samples will be obtained in the children just before starting study medication, during the first course of medication and either just prior to starting the second course of medication or 50 days following the last of the three courses of medication. Markers of immune activity in children receiving Echinacea or placebo will be compared.

Detailed description

This is an application to study the biologic activity of a specific formulation of Echinacea purpurea in children 6-11 years old. The goal of the study is to determine if Echinacea purpurea is associated with activation of immune markers including cytokines such as tumor necrosis factor alpha (TNF), interferon alpha, interferon gamma, and interleukins 2, 6, and 12 (IL-2, IL-6, and IL-12), as well CD25 and CD69 activation. A total of 40 study children will be randomized to receive either the Echinacea purpurea formulation or placebo for 10 consecutive days at the start of 3 consecutive 30-day periods. Blood samples will be obtained at baseline, at the time of peak TNF activity, and either 30 or 120 days after beginning the study medication. Prior to beginning this pediatric study peak TNF activity will be determined by administering the Echinacea purpurea to 3 adult volunteers for 10 days and doing frequent blood sampling during this period. If it is demonstrated that this formulation of E purpurea has biologic activity, a large randomized controlled trial is planned to determine if E purpurea can prevent upper respiratory tract infection (URI) in children 2-11 years old.

Interventions

BIOLOGICALEchinacea purpurea 100 mg/ml in liquid formulation

10 ml BID for 10 consecutive days at the start of 3 consecutive 30 day periods

OTHERplacebo

10 ml PO BID for 10 consecutive days at the beginning of 3 consecutive 30 day periods

Sponsors

National Center for Complementary and Integrative Health (NCCIH)
CollaboratorNIH
University of Washington
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
6 Years to 11 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy children 6-11 years old * Parent/Caregiver who can read and speak English * One child per family

Exclusion criteria

* History of allergic reaction to Echinacea or related species * History of asthma * History of allergic rhinitis * History of autoimmune disease

Design outcomes

Primary

MeasureTime frame
TNF levelsDuring first course of study medication

Secondary

MeasureTime frame
CD25/CD69 activation120 days
IL-2, IL-6, IL-12, interferon alpha, interferon gamma, TNF levels120 days
specific and general adverse events120 days

Outcome results

None listed

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