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Tracing Of Real-time glu13Cose Metabolism in Human Immune Cells

Tracing Of Real-time glu13Cose Metabolism in Human Immune Cells

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06930976
Acronym
TORCH
Enrollment
12
Registered
2025-04-16
Start date
2025-10-01
Completion date
2027-06-30
Last updated
2025-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glucose, Immune System and Related Disorders, Isotope Labeling, Metabolism

Brief summary

The purpose of this study is to understand how cells of the immune system use the common sugar glucose to fuel energy production and as a building block within the cell. Investigators will intravenously infuse a non-radioactive glucose tracer into participants over a few hours and collect immune cells from the blood to track uptake and usage of this glucose within these immune cells.

Interventions

Compounded as 5% 13C6-Glucose in sterile water given IV over 2-4 hours as a split bolus and infusion

Sponsors

Vanderbilt University Medical Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adults aged 18 or older

Exclusion criteria

* Pregnant * Prisoner or in police custody * Uncontrolled hyperglycemia/diabetes * Current participation in another study where the total volume of blood drawn, when added to this study blood draw volume, exceeds 500cc in an 8 week period * Any medical issue or pharmacologic exposure which, in the opinion of the study investigator, that might interfere with the study objectives * Any reason which, in the opinion of the study investigator, adds additional risk to the participant

Design outcomes

Primary

MeasureTime frameDescription
13C6-glucose uptake in immune cellsUp to 4 hoursDetection of 13C6-glucose-derived metabolites in neutrophils, monocytes, CD4 T cells, and CD8 T cells using gas and liquid chromatography-mass spectrometry (GC-MS and LC-MS) following magnetic enrichment of these immune cell subsets.

Countries

United States

Contacts

Primary ContactMatthew T Stier, M.D., Ph.D.
matthew.stier@vumc.org615-875-4978

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026