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Effects of Nutritional Support on Postoperative Delirium

Effects of Nutritional Support on Postoperative Delirium (POD) in Elderly Non-cardiac Surgical patients_non-inferiority Comparison

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06467552
Enrollment
314
Registered
2024-06-21
Start date
2024-06-30
Completion date
2028-05-12
Last updated
2024-06-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Delirium

Brief summary

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.

Interventions

PROCEDUREcontrol group

The entire process is carried out according to Severance Hospital surgical protocols.

DIETARY_SUPPLEMENTNucare Curact group

The entire process is carried out according to Severance Hospital surgical protocols. The patients of control group will receive education from the research team about the importance of nutrition and exercise before and after surgery. In addition, the patients of control group will be instructed to take up to 4 doses of the nutritional supplement (Nucare Curact provided by DAESANG Wellife Inc.) per day for approximately 2 weeks before surgery and for about 4 weeks after surgery.

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* 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.

Exclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
incidence of postoperative deliriumfrom postoperative day 0 to postoperative day 7Confusion assessment methods(CAM) will be used for diagnosing delirium At least two times a day during the hospitalization period. Patients diagnosed with delirium using the CAM were evaluated for the duration, symptoms, and type of delirium (e.g., reduced awareness of the environment; poor cognitive skills; behavioral changes; and emotional disturbances). \*\* Confusion assessment methods(CAM) diagnostic algorism (positive or negative result, positive means delirium) CAM is considered positive if features 1 and 2 are present, with at least one of features 3 or 4. Below are the four criteria of features : 1. Acute onset and fluctuating course Determined by collateral history or repeated clinic assessment 2. Inattention Counting from 20-1 is a simple (if blunt) test for this 3. Disorganized thinking 4. Altered levels of consciousness

Secondary

MeasureTime frameDescription
type of deliriumfrom postoperative day 0 to postoperative day 7
K-FRAIL for frailtyfrom postoperative day 0 to postoperative day 7The Korean version of the fatigue, resistance, ambulation, illnesses, and loss of weight (K-FRAIL) scale : 0(healthy)\ 8(frail). A raw score is standardized. A lower score means cognitive dysfunction.
GDS for depressionfrom postoperative day 0 to postoperative day 7Geriatric Depression Scale(GDS) : 0(normal)\ 15(depression). A raw score is standardized. A lower score means cognitive dysfunction.
ADL for independencefrom postoperative day 0 to postoperative day 7Activities of Daily Living(ADL)-Barthel Index : 0(completely dependent )\ 105( independent). A raw score is standardized. A lower score means cognitive dysfunction.
duration of deliriumfrom postoperative day 0 to postoperative day 7The Quality of Recovery-40 (QoR-40) : 40\ 200(better recovery)
QOR-40 for recoveryfrom postoperative day 0 to postoperative day 7The Quality of Recovery-40 (QoR-40) : 40\ 200(better recovery)
K-MoCA for cognitive dysfunctionfrom postoperative day 0 to postoperative day 7Korean-Montreal Cognitive Assessment(K-MoCA) : 0\ 30, cognitive dysfunction\<23.
IADL for independencefrom postoperative day 0 to postoperative day 7Instrumental Activities of Daily Living(IADL)-Lawton-Brody Scale : 0\ 8(complete independence).
SNSB-c for cognitive dysfunctionfrom postoperative day 0 to postoperative day 7Seoul Neuropsychological Screening Battery-Core(SNSB-C): total score is 617. A raw score is standardized. A lower score means cognitive dysfunction.

Countries

South Korea

Contacts

Primary ContactBon-Nyeo koo, MD
koobn@yuhs.ac82-10-9982-4469

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026