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Clinical Trials in Turkey / NCT07374055
Active, not recruiting Observational

The Effect of Nutritional Status on Postoperative Mortality and Morbidity in the Geriatric Population Undergoing Gastrointestinal Surgery

NCT07374055 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2025-02-01
Last updated
2026-01-30

Condition(s) studied

Nutrition AssessmentGeriatric Anesthesia

Investigational drug(s) / intervention(s)

Preoperative Risk ScoringPostoperative Morbidite and Mortality MonitoringDelirium Assessment Protocol

Preoperative Risk Scoring: Patients will be evaluated preoperatively using three distinct scoring systems: the Geriatric Nutritional Risk Index (GNRI), the Mini Nutritional Assessment-Short Form (mNA-SF), and the Systemic Immune-Inflammation Index (SII). These scores are calculated based on serum albumin levels, body weight, a 6-question survey, and laboratory values (platelets, neutrophils, and lymphocytes).

Postoperative Morbidite and Mortality Monitoring: Systematic tracking of postoperative outcomes including hospital and ICU stay duration, pulmonary complications (e.g., pneumonia, embolism), extrapulmonary complications (e.g., surgical site infection, organ failure, delirium), and mortality rates at 30, 60, and 90 days.

Delirium Assessment Protocol: Patients will be monitored for delirium preoperatively, on the first postoperative day, and before discharge using the Confusion Assessment Method (CAM/CAM-ICU) and the Richmond Agitation-Sedation Scale (RASS).

Study summary

The purpose of this study was to compare the sensitivity and specificity of the Geriatric Nutritional Risk Index (GNRI), Mini Nutritional Assessment Scale-Short Form (mNA-SF) and Systemic Immune-Inflammatory Index (SII) values calculated in the preoperative evaluation in patients over 65 years of age who underwent gastrointestinal surgery, in predicting morbidity and mortality in the postoperative period.

Eligibility

Sex
ALL
Min age
65 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients scheduled to undergo gastrointestinal surgery. Age 65 years and older. ASA (American Society of Anesthesiologists) physical status class 3 or 4. Mini-Mental State Examination (MMSE) score of 21 or higher Exclusion Criteria: * Patients who do not consent to participate in the study. Patients with acute infection during the preoperative period. Patients who received albumin replacement in the preoperative period. Patients with a Mini-Mental State Examination (MMSE) score below 21.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kartal Dr. Lutfi Kirdar City Hospital Istanbul Kartal

More Dr. Lutfi Kirdar Kartal Training and Research Hospital trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07374055 on ClinicalTrials.gov ↗ ← All trials in Turkey