RecruitingNot Applicable

Hunger Perception and Weight-Related Outcomes Following Use of a Leptin-Supporting Dietary Supplement

United States100 participantsStarted 2025-09-10

Plain-language summary

This study evaluates changes in hunger perception and body composition-related measures following daily use of a commercially available dietary supplement formulated to support leptin-related metabolic signaling. Adult participants will self-administer the supplement for 12 weeks and complete periodic self-reported assessments related to appetite, hunger, and weight-related outcomes. Participants serve as their own control, with comparisons made between baseline and follow-up measurements. The study is designed to generate preliminary, real-world evidence regarding supplement use in a general wellness context.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Adults aged 18 years or older * Willing to pay for study supplies and able to take the dietary supplement daily for 12 weeks * Willing to complete electronic questionnaires and self-reported measurements * Able to provide informed consent Exclusion Criteria: * Pregnant or breastfeeding individuals * Known allergy or sensitivity to any supplement ingredients * Use of medications or supplements that could interfere with appetite or weight without medical clearance * Any medical condition that would make participation unsafe, as determined by the participant

What they're measuring

Change in Hunger Perception

Timeframe: Baseline and Week 12

Trial details

NCT IDNCT07442864

SponsorEfforia, Inc

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2026-09-10

Contact for this trial

Matthew Amsden

646-679-2479 help@efforia.com

View on ClinicalTrials.gov More Hunger trials