Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
ID07215351

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

N/A

Total Duration

On this page

Sponsors

U

University of Memphis

Lead Sponsor

I

INNOSUPPS

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are investigating the effects of a natural dietary supplement called Inno Cleanse™ on reducing bloating in healthy adults who frequently experience this symptom. The study also aims to evaluate potential benefits such as weight loss and improved skin health. Despite its popularity and positive reviews, there is currently no clinical research supporting Inno Cleanse's effectiveness. This trial is a double-blind, placebo-controlled study conducted by the University of Memphis to provide scientific evidence about the supplement's impact. Participants will be randomly assigned to one of two groups. One group will take two capsules daily of the Inno Cleanse dietary supplement, which contains various herbal ingredients and natural powders, for two weeks. The other group will receive two capsules daily of a placebo with inactive ingredients for the same duration. Assessments will be conducted before and after the intervention period to compare effects between the groups. Throughout the study, participants will undergo a variety of evaluations including mood questionnaires, physical measurements like weight and body circumference, and blood and urine tests to monitor safety. They will also maintain food diaries and report on bowel habits using the Bristol Chart. The study will measure many blood and urine markers at baseline and after two weeks to assess health changes. Participant involvement lasts for two weeks of treatment with assessments before and after this period.

CONDITIONS

Brief 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
  • Adults aged 18 years or older
Not Eligible

You will not qualify if you...

  • Pregnant, planning to become pregnant, or breastfeeding
  • Allergic or sensitive to any ingredient in the study product or placebo
  • History of severe allergic reactions requiring emergency care
  • Diagnosed with digestive disorders such as celiac disease, Crohn's disease, GERD, IBS, ulcerative colitis, or ulcers
  • Experiencing regular diarrhea
  • 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 affect gut health, including diuretics, laxatives, antidiarrheal, anticholinergic, or antispasmodic agents
  • Previous adverse reactions to laxatives
  • Taking medications known to interact with the supplement ingredients, including blood pressure meds, blood thinners, cholesterol meds, NSAIDs, insulin, corticosteroids, and others
  • Tobacco user
  • Engaged in strenuous activity within 24 hours before testing visits
  • Consumed caffeine or alcohol within 24 hours before testing visits

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 2 weeks

Participants take 2 capsules daily of either the experimental dietary supplement or placebo for digestive health.

1 baseline visit and 1 follow-up visit

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

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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