No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
150 (estimated)
Sponsor
Viome · Industry
Who this trial is looking for
This trial is looking for adults with diabetes or prediabetes who want to lower their blood sugar levels. Participants will follow Viome's nutrition program and visit a testing center for screenings.
Are You a Good Fit for This Trial?
Must not be takingSulfonylureasExogenous insulin
You may be able to join if
I am 18 years old or older
I can read and speak English
My HbA1c is between 5.7-8.9%
I am willing to follow the trial's instructions
I can visit a Quest Diagnostic Patient Service Center
I have signed an informed consent form
I can use a smartphone and the Viome app
You may not be able to join if
I have used antibiotics in the past month
I have been pregnant in the last 6 months
I currently use medications that increase insulin
I have used insulin in the past
I have followed a specific diet to lower my blood sugar in the last month
I take diet pills
I am allergic to an ingredient in the trial products
I have plans for significant surgery or a major medical procedure
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
This is a randomized, placebo-controlled trial that will test the efficacy of VPNP in reducing HbA1c. Participant recruitment will occur through direct-to-participant enrollment. No additional clinical sites will be used for recruitment.
Trial Locations
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City
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Status
Eligibility Criteria
Inclusion Criteria:
* Signed and dated informed consent form and medical release prior to any trial-specific procedures are performed
* Females and males aged 18 years or older
* Able to speak and read English
* HbA1c between 5.7-8.9% (inclusive), tested within the past 30 days
* Willing and able t…
Inclusion Criteria:
* Signed and dated informed consent form and medical release prior to any trial-specific procedures are performed
* Females and males aged 18 years or older
* Able to speak and read English
* HbA1c between 5.7-8.9% (inclusive), tested within the past 30 days
* Willing and able to visit a Quest Diagnostic Patient Service Center (PSC)
* Willing and able to follow the trial instructions and Viome's Precision Nutrition Program
* Willing and able to use a smartphone and Viome app.
Exclusion Criteria:
* Antibiotic use within one month of the GI test
* Gestation within previous 6 month
* Current (or previous) use of medications that increase insulin (sulfonylureas, such as glimepiride, glipizide, glyburide, etc.)
* Current (or previous) use of exogenous insulin (such as Tresiba, Lantus, Toujeo, Levemir, Humalog, Novolog, Apidra, Fiasp, etc.)
* On a specific diet, such as ketogenic, for the purpose of reducing HbA1c and/or weight within the previous month
* Taking diet pills
* Allergy to an ingredient in the MH capsule or stick pack
* Currently on an investigational product
* Significant surgery or medical procedure planned
* Diet or lifestyle change during the trial period, besides those appropriate for trial arm Has followed Viome nutritional recommendations (foods and/or supplements)
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