Actively Recruiting

Age: 18Years +
All Genders
ID07542925

Comparison of ASA, SORT, CACI, and P-POSSUM Scores for Predicting Postoperative Intensive Care Unit Requirement in Patients Undergoing Oncologic Surgery

Led by Dr Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital · Updated on 2026-04-21

500

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating how well different risk scoring systems predict the need for intensive care unit (ICU) admission after surgery in adults undergoing cancer-related operations. This study focuses on adult patients having elective or emergency oncologic surgery and aims to improve patient safety and the use of ICU resources by identifying those likely to need critical care postoperatively. The trial is a single-center, prospective observational cohort study enrolling 500 participants. Participants will undergo standard oncologic surgery, and their preoperative clinical data, intraoperative variables, and perioperative characteristics will be collected. The study assesses several risk scores including ASA Physical Status, Surgical Outcome Risk Tool (SORT), Age-adjusted Charlson Comorbidity Index (CACI), Portsmouth Physiological and Operative Severity Score (P-POSSUM), Eastern Cooperative Oncology Group (ECOG) performance status, Nutritional Risk Screening 2002 (NRS-2002), and serum albumin levels. These scores will be compared to see how well they predict ICU admission within 24 hours after surgery. During the study, researchers will record preoperative and surgical data and monitor patients for ICU admission and other outcomes such as unplanned ICU stays, mechanical ventilation needs, ICU and hospital length of stay, and mortality within 30 days. The main measurement is the rate of unplanned ICU admission within 24 hours post-surgery. Data will be analyzed using statistical models to evaluate the accuracy of each scoring system. Participants will be followed through their hospital stay and up to 30 days after surgery to determine these outcomes.

CONDITIONS

Brief Title

Prediction of Postoperative ICU Requirement in Oncologic Surgery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years and older
  • Patients scheduled for elective or emergency oncologic surgery
  • Patients who are able to provide written informed consent
  • Patients whose data will be analyzed for both planned and unplanned intensive care unit (ICU) admissions
Not Eligible

You will not qualify if you...

  • Patients under 18 years of age
  • Patients requiring continuous ICU follow-up due to a pre-existing critical illness prior to the current surgery
  • Patients who do not provide consent to participate in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 90 days post-surgery

Participants undergoing oncologic surgery are observed with collection of preoperative, intraoperative, and postoperative data to evaluate risk scoring systems and need for intensive care.

Visits occur around the time of surgery and during hospital stay up to 90 days

Trial Site Locations

Total: 1 location

1

Dr. Abdurrahman Yurtaslan Oncology Training and Research Hospital

Ankara, Turkey (Türkiye)

Actively Recruiting

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Research Team

B

Busra Uslu YAMAN

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

ICU Admission, Discharge, and Triage Guidelines: A Framework to Enhance Clinical Operations, Development of Institutional Policies, and Further Research.

Joseph L Nates, Mark Nunnally, Ruth Kleinpell...

https://pubmed.ncbi.nlm.nih.gov/27428118