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Changes in Resting Metabolic Rate Following Orthopedic Surgery

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University of Kansas

Status

Enrolling

Conditions

Metabolism; Disorder, Postprocedural
Resting Metabolic Rate
Post Operative Nutrition

Treatments

Other: Post-surgical nutrition, hydration, RMR and body composition assessments
Other: Pre-surgical nutrition, hydration, RMR, and body composition assessments

Study type

Observational

Funder types

Other

Identifiers

NCT06107959
STUDY00150689

Details and patient eligibility

About

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.

Full description

Surgery produces a catabolic response in the body that shifts metabolism from glucose to fat and protein. Despite no studies examining ACLR, studies of other orthopedic surgeries demonstrate increased postoperative energy expenditure, as well as a shift to beta-oxidation. Additionally, in most patients, these changes reverted to baseline within six weeks, although a subset of patients did not return to baseline until beyond 12 weeks.

This project will improve our understanding of magnitude and duration of RMR changes following orthopedic surgery, and the subsequent perioperative dietary suggestions that should be made to improve patient outcomes. Currently, postoperative dietary suggestions are not surgery nor patient specific. Determining how orthopedic surgery effects RMR will help to personalize perioperative treatment, rehabilitation, and recovery.

Better understanding the change in RMR following orthopedic surgery and implementing more accurate dietary modifications will help to ensure positive outcomes and control of infection following orthopedic surgery.

Enrollment

100 estimated patients

Sex

All

Ages

15+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Any individual over 15 undergoing an orthopedic surgery.

Exclusion criteria

  • Pregnant female
  • < 15 years old

Trial design

100 participants in 2 patient groups

Male
Description:
50 male subjects undergoing orthopedic surgery.
Treatment:
Other: Pre-surgical nutrition, hydration, RMR, and body composition assessments
Other: Post-surgical nutrition, hydration, RMR and body composition assessments
Female
Description:
50 female subjects undergoing orthopedic surgery
Treatment:
Other: Pre-surgical nutrition, hydration, RMR, and body composition assessments
Other: Post-surgical nutrition, hydration, RMR and body composition assessments

Trial contacts and locations

1

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Central trial contact

Sharon Bradshaw

Data sourced from clinicaltrials.gov

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