Clinical Trial

Continuous Enteral Feeding Until Tracheostomy and Aspiration Risk

Completed
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Summary
This prospective observational study evaluates whether continuing enteral feeding until tracheostomy affects aspiration pneumonia risk and early clinical outcomes in mechanically ventilated intensive care unit patients undergoing elective percutaneous tracheostomy. Patients are managed according to routine ICU practice and are observed in two groups: those who continue enteral feeding until tracheostomy preparation and those who undergo conventional 6-8-hour fasting before the procedure. The primary outcome is the incidence of aspiration pneumonia within 72 hours after tracheostomy. Secondary outcomes include respiratory parameters, arterial blood gas values, procedure-related complications, length of stay, and mortality. The study aims to determine whether routine fasting before tracheostomy provides additional clinical benefit or whether maintaining nutritional continuity may be a safe alternative in critically ill patients.
Trial Details
NCT Number NCT07508293
Lead Sponsor Bursa Yuksek Ihtisas Training and Research Hospital
Conditions Aspiration Pneumonia, Tracheostomy, Mechanical Ventilation
Enrollment 91 participants
Start Date 2022-12-16
Primary Completion 2023-12-01 (estimated)
Study Completion 2024-01-01 (estimated)
Updated on ClinicalTrials.gov 2026-04-02