Ireland
--:--IST
Recruiting Observational

The Effect of Perioperative Nutritional Care on Recovery After Knee and Hip Replacement Surgery

NCT06989229 · tracked via the Priya Life Science Czechia tracker
Phase
Observational
Started
2025-05-01
Last updated
2026-10-13

Condition(s) studied

Postoperative OutcomesPostoperative ComplicationsLength of Hospital Stay

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Elective total hip replacement Elective total knee replacement Exclusion Criteria: Hip fracture Diabetes mellitus 1 Insulinotherapy

Primary outcome measure(s)

  • Incidence of Postoperative Complications — 2 weeks postoperatively
    Measurement: Number and type of complications documented in the patient's medical records during hospitalization and up to discharge, including infections, aspiration, and other clinical events.

Trial sites (1)

FacilityCityRegionStatus
First Department of Orthopaedic Surgery, St. Anne's University Hospital and Faculty of Medicine, Masaryk University, Brno, Czechia Brno Czechia Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06989229 on ClinicalTrials.gov ↗ ← All trials in Czechia