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Study identifier: NCT07336160 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

ERAS-Based Preoperative Nutrition and Fasting in Total Knee Arthroplasty

Condition: Total Knee Arthroplasty · Postoperative Nausea and Vomiting  ·  Sponsor: Nermin Ocaktan

PhaseNA
Planned participants72
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Nermin Ocaktan, PhD  ·  +905337373306  ·  nermin.ocaktan@acibadem.edu.tr

Always discuss trial participation with your own doctor first.

Locations (1)

Acıbadem Health Group Atakent HospitalIstanbul, Istanbul, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07336160