NCT06107959 Changes in Resting Metabolic Rate Following Orthopedic Surgery
| NCT ID | NCT06107959 |
| Status | Recruiting |
| Phase | — |
| Sponsor | University of Kansas Medical Center |
| Condition | Metabolism; Disorder, Postprocedural |
| Study Type | OBSERVATIONAL |
| Enrollment | 100 participants |
| Start Date | 2023-10-10 |
| Primary Completion | 2027-06 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 100 participants in total. It began in 2023-10-10 with a primary completion date of 2027-06.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
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
Inclusion Criteria: * Any individual over 15 undergoing an orthopedic surgery. Exclusion Criteria: * Pregnant female * \< 15 years old
Contact & Investigator
Frequently Asked Questions
Who can join the NCT06107959 clinical trial?
This trial is open to participants of all sexes, aged 15 Years or older, studying Metabolism; Disorder, Postprocedural. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06107959 currently recruiting?
Yes, NCT06107959 is actively recruiting participants. Contact the research team at sbradshaw2@kumc.edu for enrollment information.
Where is the NCT06107959 trial being conducted?
This trial is being conducted at Kansas City, United States.
Who is sponsoring the NCT06107959 clinical trial?
NCT06107959 is sponsored by University of Kansas Medical Center. The trial plans to enroll 100 participants.