Actively Recruiting
GUSS-ICU Safe Nutrition Program After Extubation in ICU Patients
Led by Istanbul University - Cerrahpasa · Updated on 2025-09-26
82
Participants Needed
2
Research Sites
68 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of this study is to evaluate the effects of using the GUSS-ICU Safe Nutrition Program after extubation in Intensive Care Unit patients. This randomized controlled trial will be conducted in the Anesthesia Intensive Care Unit of Bakırköy Dr. Sadi Konuk Training and Research Hospital. Eligible participants will be randomly assigned to either the control group (usual care/routine follow-up group) or the intervention group (GUSS-ICU patients). Patients undergoing GUSS-ICU assessment will continue the nutritional program, as directed by the scale, for four days. Data are recorded on the first and last day. The data will then be evaluated in conjunction with the control group data.
CONDITIONS
Official Title
GUSS-ICU Safe Nutrition Program After Extubation in ICU Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 and over
- Patients expected to remain intubated for more than 24 hours
- Patients who have been extubated for no more than 4 hours
You will not qualify if you...
- Patients with neuromuscular disease
- Patients requiring non-invasive ventilation for more than 6 hours after extubation
- Patients being followed in the terminal phase
- Patients with a tracheostomy cannula
- Patients with a history of dysphagia
- Patients with head or neck cancer or surgery
- Patients with existing facial fractures
- Patients with a RASS score not within the 0-2 range
- Patients at high risk of bleeding (INR ≥ 2.0, Platelet count ≤ 50,000)
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Trial Site Locations
Total: 2 locations
1
Bakırköy Dr. Sadi Konuk Training and Research Hospital
Istanbul, Turkey (Türkiye)
Actively Recruiting
2
Istanbul Universitesi-Cerrahpasa
Istanbul, Turkey (Türkiye)
Actively Recruiting
Research Team
M
Merve TURKAY
CONTACT
Z
Zeliha TÜLEK
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
2
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