Actively Recruiting
Oral Nutritional Optimization in Total Joint Arthroplasty
Led by NYU Langone Health · Updated on 2025-09-11
72
Participants Needed
2
Research Sites
312 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this study is to determine the effect on hematological markers of nutritional intervention on nutritionally deficient patients following total joint replacement surgery.
CONDITIONS
Official Title
Oral Nutritional Optimization in Total Joint Arthroplasty
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who are candidates for elective primary total hip or knee replacement surgery
- Patients aged 55 to 95 years
- Patients with at least one laboratory indicator of malnutrition: serum albumin 6lt;= 3.5 mg/dl, pre-albumin 6lt; 15 mg/dl, or transferrin 6lt; 200 mg/dl
You will not qualify if you...
- History of septic arthritis
- Allergy to oral nutritional supplements
- Unable to consume oral nutritional supplements
- Protein malabsorption syndromes
- Eating disorders
- End stage kidney or liver disease
- Revision surgery, urgent surgery, hemiarthroplasty, or partial knee replacement
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
NYU Langone Health
New York, New York, United States, 10016
Actively Recruiting
2
Rothman Orthopedic Institute
Philadelphia, Pennsylvania, United States, 19107
Actively Recruiting
Research Team
D
Daniel Waren
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here