Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06582381

Evaluation of Biomarkers for Predicting Macronutrient Intake

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
33 (estimated)
Sponsor
Texas A&M University · Academic / Other
Sex
All
Age
50 Years – 75 Years
Healthy volunteers
Accepted

Summary

The goal of this clinical trial is to establish the relationship between macronutrient food intake and the resulting blood and intersticial fluid (ISF )levels of small molecule markers, as well as, validate wearable optical readers and data fusion algorithms to accurately predict individual-specific macronutrient availability in real time. The study involves 1 screening visit of approximately 2 hours and up to 4 study days of approximately 14 hours. Subjects will be asked to arrive in the fasted state on all study days. Fasting prior to screening is not required. On the screening visit, body weight, height, and body composition by Dual-energy X-ray absorptiometry (DXA) will be measured. In addition, habitual dietary intake, physical activity level (PASE), and quality of life (SGRQ-C) will be assessed.

Detailed description

On each study day, body weight and height will be measured. An in-dwelling catheter will be inserted in a peripheral vein of the lower arm or hand to enable blood sampling. The arm will be put in a hot box to allow collecting arterialized venous blood samples. After taking a baseline blood sample, the predefined meal will be consumed within 10 min. Small arterialized venous blood samples (5 ml) will subsequently be drawn multiple times. Samples will be collected in predefined tubes, plasma/serum separated, aliquoted, and stored at -80 deg. Celsius for later assays and/or send to a local accredited laboratory for the concentrations of amino acids and other parameters (including amino acids, fatty acids, glucose, insulin). In the opposite limb, a commercially available microdialysis catheter will be placed in the forearm following standard operating procedures developed by the European Academy of Allergy \& Clinical Immunology Task Force on Skin Microdialysis. Dialysate will be collected in 30-minute aliquots in microvials for the duration of the study day. Microvials will be weighed before and after sample collection. A syringe filled with perfusate containing mixture of stable tracer-labelled amino acids and glucose will be infused through the syringe pump at a controlled rate. On each of the study days, subjects will consume two meals with defined composition of macronutrients eight hours apart.

Conditions

Interventions

TypeNameDescription
OTHERMeal set Amorning meal: low carbohydrate, low protein, low fat afternoon meal: high carbohydrate, high protein, high fat
OTHERMeal set Bmorning meal: low carbohydrate, high protien, low fat meal afternoon meal: high carbohydrate, low protein, high fat meal
OTHERMeal set Cmorning meal: low carbohydrate, low protien, low fat meal afternoon meal: high carbohydrate, high protein, low fat meal
OTHERMeal set Dmorning meal: high carbohydrate, low protien, low fat meal afternoon meal: low carbohydrate, high protein, high fat meal

Timeline

Start date
2023-12-06
Primary completion
2026-01-01
Completion
2026-12-01
First posted
2024-09-03
Last updated
2025-07-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06582381. Inclusion in this directory is not an endorsement.