A Clinical Trial to Assess the Efficacy and Tolerance of a Berberine-based Nutraceutical Formula to Aid Blood Sugar Regulation and Metabolism

Recruiting now · Not applicable · Has a placebo group

Conditions studied: Metabolism Disorder, Nutraceutical

In brief

This randomized, triple-blind, placebo-controlled study will evaluate the efficacy of Diaberine, a berberine-based nutraceutical, in aiding blood sugar regulation and metabolism in 80 participants over 24 weeks.

Key facts

Study ID: NCT06700915
Run by: Ultimate International, Inc.
People needed: 80
Starts: 2024-10-03
Expected to finish: 2025-05-01
Last updated by the study team: 2024-12-13

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Male or female.
BMI: 27-35 kg/m2
HbA1c of 5.7%-6.4% (determined by prescreening blood test)
Be generally healthy
Willing to refrain from taking any products, prescription medications, or supplements that target blood sugar regulation or metabolism during the test period.
Willing to maintain their current diet, sleep schedule, and activity level for the duration of the study.

You may not qualify if…

Diagnosed with Type 2 diabetes mellitus (T2DM) and have been prescribed metformin, insulin, Sulfonylureas, Meglitinides, SGLT2 inhibitors and/or GLP-1 medications including the following prescription medications: Wegovy (semaglutide), Ozempic (semaglutide), Rybelsus (semaglutide), Saxenda (liraglutide), Victoza (liraglutide), Zepbound (bimagrumab), Byetta (exenatide), Bydureon (exenatide ER), Trulicity (dulaglutide), Adlyxin (lixisenatide)
Current use or past history of use within the last 2 months (8 weeks) of the following prescription medications: Beta-blockers Sectral (Acebutolol), Tenormin (Atenolol), Kerlone, Betoptic (Betaxolol), Zebeta (Bisoprolol), Coreg, Coreg CR (Carvedilol), Trandate, Normodyne (Labetalol), Lopressor, Toprol XL (Metoprolol), Corgard (Nadolol), Bystolic (Nebivolol), Levatol (Penbutolol), Visken (Pindolol), Inderal, Inderal LA, InnoPran XL (Propranolol). Thiazide diuretics Diuril (Chlorothiazide), Microzide (Hydrochlorothiazide), Thalitone, Hygroton (Chlorthalidone), Lozol (Indapamide), Zaroxolyn (Metolazone), Naturetin (Bendroflumethiazide), Enduron (Methyclothiazide). Corticosteroids Deltasone (Prednisone), Orapred, Prelone (Prednisolone), Medrol (Methylprednisolone), Qvar (Beclomethasone), Celestone (Betamethasone), Decadron (Dexamethasone), Cortef (Hydrocortisone), Kenalog (Triamcinolone). Immunosuppressants Tacrolimus (Prograf), Cyclosporine (Neoral), Sirolimus (Rapamune)
Women who are pregnant, breastfeeding, or trying to conceive.
Anyone unwilling or unable to follow the study protocol.
Any pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders.
Is currently undergoing or planning to undergo any significant medical procedures in the next six months
Has had any major illness in the last three months.
A history of severe allergic reactions, including but not limited to any of the product's ingredients.
Heavy drinkers or drug users. A heavy drinker is considered to be a woman who drinks 8 or more alcoholic drinks per week or a man who drinks 15 or more alcoholic drinks per week.
Impaired hepatic function.
Individuals taking prescription or over-the-counter medication, or herbal remedies that affect blood sugar regulation or metabolism.
Currently being treated for an infection with an antibiotic and/or antiviral prescription medication.

Where it is running

Citruslabs — Santa Monica, California, United States (enrolling)

Full record on ClinicalTrials.gov

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