Actively Recruiting
The Effect of Perioperative Nutritional Care on Recovery After Knee and Hip Replacement Surgery
Led by St. Anne's University Hospital Brno, Czech Republic · Updated on 2025-05-25
1000
Participants Needed
1
Research Sites
139 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This prospective observational study will assess the impact of standardized perioperative nutritional care on postoperative outcomes in patients undergoing elective total hip (THA) or knee arthroplasty (TKA) at the First Department of Orthopaedic Surgery, St. Anne's University Hospital in Brno. The protocol includes preoperative patient education, nutritional risk screening, and carbohydrate loading up to two hours before anesthesia, followed by early postoperative refeeding. Data collection will include demographic and surgical variables, nutritional status, carbohydrate intake, and the occurrence of intra- and postoperative complications, including infection and delayed wound healing. As perioperative nutritional care is part of routine clinical practice, the study requires no additional interventions or resources. Results will provide evidence on the effectiveness of structured nutritional support in enhancing recovery and reducing complications after joint replacement surgery.
CONDITIONS
Official Title
The Effect of Perioperative Nutritional Care on Recovery After Knee and Hip Replacement Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Elective total hip replacement
- Elective total knee replacement
You will not qualify if you...
- Hip fracture
- Diabetes mellitus type 1 treated with insulin therapy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
First Department of Orthopaedic Surgery, St. Anne's University Hospital and Faculty of Medicine, Masaryk University, Brno, Czechia
Brno, Czechia, Czechia, 60200
Actively Recruiting
Research Team
V
Vasileios Apostolopoulos, M.D., Ph.D.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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