Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07215351

Impact of the Inno Cleanse Dietary Supplement on Gut Health and Associated Variables in Healthy Men and Women

Led by University of Memphis · Updated on 2026-04-02

30

Participants Needed

1

Research Sites

29 weeks

Total Duration

On this page

Sponsors

U

University of Memphis

Lead Sponsor

I

INNOSUPPS

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of the present study is to investigate the impact of a natural dietary supplement, Inno Cleanse™, to reduce bloating in a population of otherwise healthy men and women, who claim to feel frequently bloated. Inno CleanseTM dietary supplement is manufactured in the United States under current Good Manufacturing Practices (cGMP) and is marketed by InnoSupps as a digestive health aid. It is sold in the United States on the company's website, Amazon, and in many large retail outlets. It remains a very popular product, with close to 1.4 million units sold since 2020, with a reported 66,000 units sold in the past three months. Despite the prevalence of dietary supplements identifying as digestive aids, detoxification, and cleanses, very little research has been done to determine their effectiveness. The product appears to be well-designed, with multiple ingredients included which have scientific evidence of effectiveness. That said, and despite the overall positive reviews, there is no known clinical research to support the product's effectiveness. Therefore, the aim of this study is to evaluate the efficacy of the Inno Cleanse product to reduce bloating and result in other positive outcomes (weight loss). This study will be run as a double-blind placebo-controlled trial, in which subjects will use the product or placebo for two weeks. It is hypothesized that treatment with the dietary supplement Inno Cleanse will result in reduced bloating, as evidenced by self-reported reductions in bloating and hunger, as well as moderate weight loss and a reduction in body circumference measures due to the reduced bloating. In addition, multiple anecdotal reports of improved skin health have been noted in those using the product. Additionally, routine blood and urine sample analysis will be performed as a secondary outcome, as a safety measure.

CONDITIONS

Official Title

Impact of the Inno Cleanse Dietary Supplement on Gut Health and Associated Variables in Healthy Men and Women

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Experience regular bloating or constipation at least 2 days per week
  • Able to fast for at least 12 hours before testing visits
  • Age 18 years or older
Not Eligible

You will not qualify if you...

  • Pregnant, planning pregnancy, or breastfeeding
  • Allergic or sensitive to any ingredients of the study product
  • History of severe allergic reactions requiring emergency care
  • Diagnosed with digestive or gut-related diseases such as celiac disease, Crohn's disease, GERD, heartburn, IBS, ulcerative colitis, or ulcers
  • Experiencing regular diarrhea
  • Have an active infection or illness
  • Diagnosed with diabetes, hypertension, or cardiovascular disease
  • History of breast, uterine, or ovarian cancer
  • Diagnosed with uterine fibroids or endometriosis
  • Taking medications or supplements that may affect gut health including diuretics, laxatives, anti-diarrheal agents, anticholinergic or antispasmodic agents
  • Previous adverse reactions to laxatives
  • Taking medications known to interact with supplement ingredients such as blood pressure meds, blood thinners, cholesterol meds, NSAIDs, corticosteroids, insulin, and others listed
  • Tobacco user
  • Engaged in strenuous activity within 24 hours of testing visits
  • Consumed caffeine or alcohol within 24 hours of testing visits

AI-Screening

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Trial Site Locations

Total: 1 location

1

Center for Nutraceutical and Dietary Supplement Research

Memphis, Tennessee, United States, 38152

Actively Recruiting

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Research Team

J

Jacquelyn Pence, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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