A Clinical Trial to Evaluate the Effects of a Dietary Supplement on Digestive Health, Energy, and Skin Health

NCT07766408 | Completed

• 2 other identifiers: 20715legacy-20715
• Study Type: interventional
• Target: 35
• Locations: 1 country
• Sites: 1

Brief Summary

This study evaluates the effects of the Clean Nutra dietary supplement MultiMineral 102 Gummies on digestive health, energy, and skin health over an 8-week period. The trial is conducted as a single-arm, unblinded, virtual study in which all 35 enrolled participants take the test product daily. Participants will complete self-reported questionnaires at Baseline, Week 2, Week 4, Week 6, and Week 8 to assess changes in digestive health, energy levels, skin health, and overall vitality. All participants reside in the United States and will follow instructions provided by the research team throughout the study duration.

Conditions

Digestive Health; Skin Health; Energy; Vitality

Outcome Measures

Primary Outcomes (3)

• Change in Digestive Health

  Self-reported change in digestive health assessed via questionnaire

  Baseline, Week 2, Week 4, Week 6, and Week 8

• Change in Skin Health

  Self-reported change in skin health assessed via questionnaire

  Baseline, Week 2, Week 4, Week 6, and Week 8

• Change in Energy Levels

  Self-reported change in energy levels assessed via questionnaire

  Baseline, Week 2, Week 4, Week 6, and Week 8

Secondary Outcomes (4)

• Participant Perception of Effects on Digestive Health

  Baseline, Week 2, Week 4, Week 6, and Week 8

• Participant Perception of Effects on Energy

  Baseline, Week 2, Week 4, Week 6, and Week 8

• Participant Perception of Effects on Skin Health

  Baseline, Week 2, Week 4, Week 6, and Week 8

• Participant Perception of Effects on Overall Vitality

  Baseline, Week 2, Week 4, Week 6, and Week 8

Study Arms (1)

MultiMineral 102 Gummies

EXPERIMENTAL

Dietary Supplement: MultiMineral 102 Gummies

Interventions

MultiMineral 102 Gummies DIETARY_SUPPLEMENT

All participants take two MultiMineral 102 Gummies per day, both taken in the morning with food and 8 oz of water, for 8 weeks. Ingredients: Sodium 10 mg; Irish Sea Moss Extract 30:1 50 mg; Black Cumin Extract 30:1 50 mg; Burdock Root Extract 20:1 50 mg; Proprietary Blend 35 mg (Manuka Honey Powder, Elderberry Extract 4:1, Ashwagandha Extract 30:1, and Chlorella Powder).

MultiMineral 102 Gummies

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Be male or female
• Be aged 18+
• In the past four weeks, has experienced issues regarding all of the following: digestion issues, poor skin health, and low energy
• Anyone who is generally healthy - does not live with any uncontrolled chronic disease
• If taking oral over-the-counter supplements or herbal remedies targeted at digestive health, energy, or skin health, has been consistently taking these for at least 3 months prior to starting the study, and is willing to maintain this routine for the study duration
• Not planning on introducing any products or any new forms of prescription medication or supplements that target digestive health, energy, or skin health for the study duration
• Willing to keep all elements of their skincare routine the same for the duration of the study
• Has not introduced any new products to their skincare routine in the past month
• Willing to maintain current diet, sleep schedule, and activity level for the duration of the study
• Resides in the United States
• Not currently partaking in another research study and will not be partaking in any other research study for the next 8 weeks and at any point during this study's duration
• If taking prescription medication, must be willing to speak with their healthcare provider before enrolling in the study

You may not qualify if:

• Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders
• Anyone with thyroid disorders
• Anyone currently taking blood thinning (anticoagulant) medication
• Anyone with any allergies or sensitivities to any of the study product ingredients
• Any women who are pregnant, breastfeeding, or trying to conceive
• Anyone who has had any major illnesses in the last three months
• Anyone unwilling to follow the study protocol
• Has stopped using hormonal birth control in the past month
• Anyone who drinks heavily (i.e. 8 or more alcoholic drinks per week for women or 15 or more alcoholic drinks per week for men)
• Anyone with a history of substance abuse

Sponsors & Collaborators

• Clean Nutraceuticals: lead
• Citruslabs: collaborator

Study Sites (1)

Citruslabs

Las Vegas, Nevada, 89101, United States

Location

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: August 11, 2026
• First Posted: August 14, 2026
• Study Start: January 22, 2025
• Primary Completion: April 16, 2025
• Study Completion: April 16, 2025
• Last Updated: August 14, 2026

Record last verified: 2026-08

Locations

US (1)