Actively Recruiting
Effects of Nutritional Support on Postoperative Delirium
Led by Yonsei University · Updated on 2024-06-21
314
Participants Needed
1
Research Sites
205 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study is a prospective, single-center, randomized controlled trial to compare whether applying nutritional supplementation therapy before and after surgery in elderly patients aged 65 years or older undergoing non-cardiac surgery can reduce the incidence of postoperative delirium.
CONDITIONS
Official Title
Effects of Nutritional Support on Postoperative Delirium
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Elderly patients aged 65 and above
- Patients undergoing non-cardiac major surgery in thoracic surgery, lung cancer surgery, multi-level spinal surgery in neurosurgery and orthopedics, or liver cancer surgery in hepatobiliary and pancreatic surgery, under general anesthesia with an expected surgery duration of 2 hours or more
- Patients scheduled for arterial catheterization
- Patients who are able to take oral intake from postoperative day 1
You will not qualify if you...
- Patients with uncontrolled systemic conditions such as diabetes, hypertension, renal disease, liver disease, and other systemic illnesses
- Those with visual impairment
- Patients with cognitive impairment based on the Mini-Mental State Examination for Dementia Screening criteria
- Individuals experiencing difficulty in communication
- Those diagnosed with neurological disorders (such as brain hemorrhage, stroke, brain tumor, dementia, Parkinson's disease, cognitive impairment, depression, etc.)
- Patients diagnosed with alcohol or substance addiction
- Patients with cancelled scheduled surgeries
- Patients undergoing minor surgeries with expected anesthesia durations of less than 2 hours
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Yonsei University Health system, Severance Hospital
Seoul, South Korea, 03722
Actively Recruiting
Research Team
B
Bon-Nyeo koo, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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