ERAS-Based Preoperative Nutrition and Fasting in Total Knee Arthroplasty

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorNermin Ocaktan

About this trial

The aim of this randomized controlled study is to investigate the effect of implementing a preoperative nutrition education and fasting protocol prepared in accordance with Enhanced Recovery After Surgery (ERAS) guidelines during the 24-hour preoperative period on postoperative hydration status and the incidence of nausea and vomiting in patients scheduled for total knee arthroplasty.

Total knee arthroplasty is a commonly performed surgical procedure, particularly in older adults, and postoperative recovery may be negatively affected by surgical stress, anesthesia-related complications, dehydration, and postoperative nausea and vomiting. ERAS protocols emphasize the optimization of preoperative nutrition and hydration as key components to improve postoperative outcomes.

In this study, patients undergoing elective total knee arthroplasty will be randomly assigned to an intervention group or a control group. Patients in the intervention group will receive ERAS-based preoperative nutrition education and a standardized fasting protocol during the 24 hours prior to surgery, while patients in the control group will receive routine standard care.

Postoperative hydration status, nausea and vomiting severity, and fluid intake-output balance will be assessed and compared between the two groups. The findings of this study are expected to contribute to improving perioperative nursing care practices and enhancing patient recovery and comfort following total knee arthroplasty.

Eligibility criteria

Qualifiers

Adults aged 18 years and older.

Patients scheduled for elective total knee arthroplasty.

Patients expected to be hospitalized for at least 48 hours postoperatively.

Ability to communicate verbally and provide informed consent.

Disqualifiers

Presence of any chronic disease requiring fluid restriction.

Diagnosed cognitive impairment or psychiatric disorders affecting comprehension (e.g., Alzheimer's disease, dementia, psychotic disorders).

Acute conditions causing dehydration in the preoperative period (e.g., vomiting, diarrhea, excessive fluid loss).

Intraoperative complications requiring intensive care unit admission.

Trial design

Treatments tested in this trial

  • ERAS-Based Preoperative Nutrition Education and Fasting Protocol
  • Standard Preoperative Care

Treatment groups

72 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Nermin Ocaktan

Lead sponsor

Acibadem University

Sponsor institution