ACTRN12620000212954
Completed
未知
An investigation into the anxiety- and stress-relieving effects of Echinacea angustifolia (EP107™): a randomised, double-blind, placebo-controlled study
Clinical Research Australia0 sites108 target enrollmentFebruary 21, 2020
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Anxiety
- Sponsor
- Clinical Research Australia
- Enrollment
- 108
- Status
- Completed
- Last Updated
- 5 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Healthy adults (male and female) between 18 and 65
- •2\. Experiencing mild\-to\-moderate severity of stress/anxiety (score between 11 and 40 on the CUXOS)
- •3\. Stressor/anxiety has been present for greater than a month
- •4\. Medication\-free for at least 3 months. Use of analgesics (once a week) or contraceptive pill are permissible.
- •5\. Non\-smoker
- •6\. BMI between 20 and 35
- •7\. No plan to commence new treatments over study period
- •8\. Willing to provide a personally signed informed consent form detailing all pertinent aspects of the trial.
- •9\. Willing and able to take prescribed tablets for 6 weeks
Exclusion Criteria
- •1\. Alcohol consumption \> 14 standard drinks per week
- •2\. Current or 12\-month history of illicit drug abuse
- •3\. Pregnant women, women who are breastfeeding or women who intended to fall pregnant.
- •4\. Suffering from medical conditions including but not limited to: gastrointestinal disease, functional gastrointestinal disorder, diabetes, hyper/hypotension, cardiovascular disease, gallbladder disease/gallstones/biliary disease, endocrine disease, psychiatric disorder (other than mild\-to\-moderate anxiety), and neurological disease (Parkinson’s, Alzheimer’s disease, intracranial haemorrhage, head or brain injury)
- •5\. Currently taking supplements that may impact on treatment outcome
Outcomes
Primary Outcomes
Not specified
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