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Acute Appetite Hormone Response of Proprietary Beverages

NCT06966570 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2026-02-11

No results posted yet for this study

Summary

The primary objective of this study is to evaluate post-meal appetite hormones and appetite ratings, assessed using visual analog scale (VAS) questionnaires, in response to proprietary beverages in generally healthy adults.

Conditions

  • Healthy

Interventions

OTHER

Study Product A: Mixed-macronutrient beverage

Participants will consume a beverage that contains mixed macronutrients.

OTHER

Study Product B: Single-macronutrient beverage

Participants will consume a beverage that contains a single macronutrient.

Sponsors & Collaborators

  • Biofortis Clinical Research, Inc.

    collaborator INDUSTRY

  • Nlumn LLC

    collaborator UNKNOWN

  • Shaklee Corporation

    lead INDUSTRY

Principal Investigators

  • Erin Barrett, PhD · Shaklee Corporation

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
20 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-04-28
Primary Completion
2025-05-23
Completion
2025-06-11

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06966570 on ClinicalTrials.gov