Phase
Condition
N/ATreatment
125mg OEA with LipiSperse
250mg OEA with LipiSperse
Placebo
Clinical Study ID
Ages > 30 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Adults aged 30 years and older
Generally healthy
BMI 25.0-34.9 kg/m2
Able to provide informed consent
Agree to not participate in another clinical trial while enrolled in this trial
Agree not to change current diet and/or exercise frequency or intensity duringentire study period
Females using a prescribed form of birth control (e.g. oral contraceptive)
Participant's ability to participate fully and comply with demands of the studyincluding attendance at all scheduled blood collection time points
Exclusion
Exclusion Criteria:
Have a serious illness e.g. neurological disorders such as MS, kidney disease, liverdisease or heart conditions
History of any glucose or insulin regulation problem, including diabetes.
Have an unstable illness e.g. thyroid gland dysfunction, uncontrolled mood disorders (e.g., depression, anxiety, bipolar).
Diagnosed with any known metabolic or endocrine dysfunctions e.g., diabetes, NAFLD,hyperinsulinemia, hypoglycaemia.
Use of any medication or supplements that may affect any metabolic pathwayassociated with satiety (e.g., GLP-1, GIP, glucagon), glucose or insulin.
Current malignancy (excluding Basal Cell Carcinoma) or chemotherapy or radiotherapytreatment for malignancy within the previous 2 years
Significant change in diet in the past 1-month (e.g., removal of a food group orcalorie restriction)
Active smokers, nicotine use or drug (prescription or illegal substances) abuse
Chronic past and/or current alcohol use (>21 alcoholic drinks week)
Pregnant or lactating women
Allergic to any of the ingredients in active or placebo formula
Participants who are or who have participated in any other clinical trial during thepast 1 month (excludes RDC clinical trials which are to be assessed on acase-by-case basis).
Any condition which in the opinion of the investigator makes the participantunsuitable for inclusion
Regular use within the past 4 weeks of supplements containing OEA and/or LipiSperse
Study Design
Study Description
Connect with a study center
RDC Clinical
Brisbane, Queensland 4006
AustraliaActive - Recruiting
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