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Study identifier: NCT07402382 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effects of Amylopectin Chromium Blend on Whole-Body Protein Kinetics and Glucose in Peri/Post-Menopausal Women

Condition: Glucose Monitoring, Continuous · Whole Body Protein Metabolism · Peri-menopausal Women  ·  Sponsor: Nutrition 21, Inc.

PhaseNA
Planned participants60
Who can joinFemale, 40 Years to 70 Years
Healthy volunteersYes

About this study

The goal of this study is to better understand how an amylopectin chromium blend may influence whole body protein balance in women during midlife, when hormonal changes can adversely affect protein metabolism and muscle maintenance. Continuous glucose monitoring will also be used to assess glycemic control over a 24-hour period. The main questions the study aims to answer are: * Does the use of an amylopectin chromium blend in peri- and post-menopausal women help to support positive protein balance * Can the affect be achieved using a concentrated dose Researchers will compare the nutritional supplement to a placebo (amylopectin alone) to see if the amylopectin chromium blend can promote positive protein balance. A concentrated dose of the supplement will also be evaluated for comparative effectiveness. Participants will: * Consume the nutritional supplement (standard or concentrated dose) or placebo acutely after a short resistance exercise bout * Complete four in-person visits, including the single-day intervention Results from this research may help guide future nutritional strategies to support healthy aging, muscle function, and overall metabolic health.

This description comes directly from the study's public registry record.

Talk to the study team

Tim Ziegenfuss, Ph.D.  ·  330-926-6927  ·  tz@appliedhealthsciences.org

Micheal La Monica, Ph.D.  ·  330-926-6927  ·  ML@appliedhealthsciences.org

Always discuss trial participation with your own doctor first.

Locations (1)

The Center for Applied Health SciencesCanfield, Ohio, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07402382