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Recruiting NCT07317921

NCT07317921 Validating IAAO for Muscle Outcomes

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Clinical Trial Summary
NCT ID NCT07317921
Status Recruiting
Phase
Sponsor University of Toronto
Condition Protein Metabolism
Study Type INTERVENTIONAL
Enrollment 8 participants
Start Date 2025-12-01
Primary Completion 2026-03-20

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 35 Years
Study Type INTERVENTIONAL
Interventions
Protein + Stable Isotope Tracer Beverage

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 8 participants in total. It began in 2025-12-01 with a primary completion date of 2026-03-20.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Consuming dietary protein stimulates whole-body and muscle protein synthesis, the latter of which is typically measured using invasive primed constant infusions of stable isotopes with concurrent muscle biopsies. Alternative non-invasive methodologies have been developed (namely the indicator amino acid oxidation (IAAO) technique) to estimate the impact of protein ingestion on whole-body protein synthesis as a proxy for determining dietary protein requirements. Given that the IAAO technique is based on principles of protein metabolism which occur in the liver, it is unclear how representative the IAAO outcomes of whole-body protein synthesis is to skeletal muscle protein synthesis. Validation of the IAAO technique against gold-standard, biopsy-derived measures of muscle metabolism (i.e., muscle protein synthesis) would assist in mitigating the invasiveness of muscle physiology and nutrition research.

Eligibility Criteria

Inclusion Criteria: * Participants will be aged 18-35 years old * Participants will have a BMI within the normal range (i.e., 18.5-24.9) and waist-to-hip circumference ratio of \<0.95 for males and \<0.8 for circumference for females to ensure homogeneity of the sample population * Participants are willing to abide by the compliance rules of this study (e.g., abstain from extraneous physical activity 48h prior to session 4 * Self-reported regular menstrual cycle (25-35d) within the last 3 months (female participants) * Physical activity score of ≥24 units as measured by the Godin leisure time exercise questionnaire Exclusion Criteria: * Inability to adhere to any of the compliance rules judged by principal investigator * Self-reported regular tobacco or illicit drug use (e.g., growth hormone or testosterone) * Current use of hormonal contraceptives * Individuals with a history of allergy to local anesthetics (e.g., lidocaine)

Contact & Investigator

Central Contact

Sabrina T Barsky, Ph.D.

✉ sabrina.barsky@utoronto.ca

📞 16475400115

Principal Investigator

Daniel Moore, Ph.D

PRINCIPAL INVESTIGATOR

University of Toronto, Faculty of KPE

Frequently Asked Questions

Who can join the NCT07317921 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 35 Years, studying Protein Metabolism. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07317921 currently recruiting?

Yes, NCT07317921 is actively recruiting participants. Contact the research team at sabrina.barsky@utoronto.ca for enrollment information.

Where is the NCT07317921 trial being conducted?

This trial is being conducted at Toronto, Canada.

Who is sponsoring the NCT07317921 clinical trial?

NCT07317921 is sponsored by University of Toronto. The principal investigator is Daniel Moore, Ph.D at University of Toronto, Faculty of KPE. The trial plans to enroll 8 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: September 2026  ·  Data Methodology