Comparing ASA and CFS for predicting surgery outcomes in elderly patients
Comparison of ASA and CFS in Predicting Peri- and Postoperative Outcomes in Elective Patients Older Than 65 Years
This study tests whether two different methods for measuring health can better predict surgery outcomes for patients over 65 years old.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Ages | 65 Years and up |
| Sex | All |
| Sponsor | Osijek University Hospital Academic / other |
| Locations | 1 site (Osijek) |
| Trial ID | NCT05998746 on ClinicalTrials.gov |
What this trial studies
This observational study evaluates the effectiveness of the American Society of Anesthesiologists (ASA) classification and the Clinical Frailty Scale (CFS) in predicting perioperative and postoperative complications in elective surgeries for patients over 65 years old. Patients will be assessed using both classifications during preoperative examinations, and their medical histories will be reviewed after treatment to analyze outcomes. The study aims to determine which categorization better correlates with complications and length of hospital stay following surgery.
Who should consider this trial
Good fit: Ideal candidates are elective surgery patients aged 65 and older without significant mental difficulties affecting daily life.
Not a fit: Patients with earlier mental difficulties that interfere with daily life, except for those with senile dementia, may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could improve preoperative assessments and outcomes for elderly patients undergoing elective surgeries.
How similar studies have performed: Previous studies have shown that CFS correlates with complications in emergency settings, suggesting potential for success in this novel application for elective surgeries.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * All elective patients older then 65 years Exclusion Criteria: * Earlier mental difficulties that affect everyday life, senile dementia is not exclusion criteria
Where this trial is running
Osijek
- University Hospital Centre Osijek — Osijek, Croatia (Recruiting)
Study contacts
- Study coordinator: Josip Kajan, Student
- Email: jkajan@mefos.hr
- Phone: +385 98 1309 408
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.