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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03995979
Other study ID # IRB201900988 -V
Secondary ID NF/SGVHS
Status Completed
Phase N/A
First received
Last updated
Start date September 9, 2019
Est. completion date February 16, 2024

Study information

Verified date April 2024
Source University of Florida
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

There is strong scientific data that supports that short-term protein restrictive diets reduce surgical stress responses. The investigators are hoping to use the information collected from the blood serum and muscle tissue of healthy subjects to help understand the baseline and early changes in muscle energetic and cell-mediated inflammation. The study team hopes to use the data collected in this pilot study to compare with patients undergoing open abdominal aortic aneurysm (AAA) repair in a future study


Description:

Modulation of a patient's diet, specifically via short-term dietary protein restriction, can impact changes in cell energetics and dampen the normal subclinical inflammatory state. These changes can provide benchmarks for future research focused on using nutritional interventions aimed at improving the probability of a successful outcome following open aortic aneurysm surgery. The investigators will conduct a short term dietary restriction protocol to characterize these changes in a normal control cohort to be compared to patients which undergo surgery, to identify the optimal time points for sampling in the surgical population. These changes will be characterized by looking at inflammatory cells in the blood, proteins excreted in the urine, changes in microbiome signature identified by stool sample and oral swab, as well as changes in muscle energetics in small muscle biopsies.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date February 16, 2024
Est. primary completion date February 16, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Healthy volunteers between 18 and 70 years of age Exclusion Criteria: - Age less than 18 years. - The presence of any significant medical condition that might significantly confound the collection of biological data in the study including cancer, diabetes, IBD, Advanced Renal Disease, Nut Allergy - Unwilling to follow protocol - Participation in another interventional clinical trial. - Prisoners, pregnancy, or direct employees of the investigative team

Study Design


Related Conditions & MeSH terms


Intervention

Other:
4 Day Protein Restricted Diet
Subjects will follow a 4 day protein restricted diet using Scandishake® mixed with almond milk which will be provided. They may also drink water. No food, other beverages, or alcohol may be consumed. The amount of diet to be consumed will be calculated for each patient based upon resting energy expenditures plus additional energy needs. These will be consumed by the study subjects at home in an unrestricted manner, in that they may be consumed at any point of time in the day.

Locations

Country Name City State
United States Malcom Randall VA Medical Center Gainesville Florida
United States UF Health---Vascular Surgery Gainesville Florida

Sponsors (2)

Lead Sponsor Collaborator
University of Florida Malcom Randall VA Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in inflammatory cell composition A shift in the inflammatory cell composition as measured by the 10x single cell genomic analysis Day 2; Day 4; Day 7; Day 14
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