About this trial
This project is intended to determine the magnitude and duration of RMR changes in patients receiving orthopedic surgery. The result will help to guide postoperative nutrition recommendations in patients receiving orthopedic surgery.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Any individual over 15 undergoing an orthopedic surgery.
Disqualifiers
Pregnant female
< 15 years old
Trial population
Subjects will be over the age of 15 years old undergoing elective orthopedic surgery at KU Medical Center.
Trial design
Cohort
Prospective
Treatments tested in this trial
Pre-surgical nutrition, hydration, RMR, and body composition assessments
Other interventionUrine sample, InBody device platform, Metabolic cart with hood to collect RMR.
Post-surgical nutrition, hydration, RMR and body composition assessments
Other interventionSame as pre-surgical tests at 1 week, 3 weeks, 6 weeks, and 12 weeks follow up time points.
Treatment groups
Trial outcomes
Primary outcomes
To determine the magnitude of the change in RMR of patients receiving orthopedic surgery.
RMR = (9.99 X actual weight\*)+ (6.25 X height\*) - (4.92 X age) - 161\*use weight in kilograms (kilogram), height in centimeters (cm).
To observe the amount of time it takes the RMR to return to baseline.
calculation in number of weeks
Sponsors and contacts
Click on the lead sponsor to view all of their trials.