Actively Recruiting

Age: 18Years +
FEMALE
ID07287280

Comparison of Charlson Comorbidity Index and POSSUM Score for Predicting Perioperative Complications in Oncogynecologic Surgery

Led by Mahidol University · Updated on 2025-12-17

300

Participants Needed

1

Research Sites

17 weeks

Total Duration

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AI-Summary

What this Trial Is About

Gynecologic cancers are increasing worldwide, making it crucial to improve care around the time of surgery. This research compares two common tools used to predict risks during onco-gynecologic surgeries: the Charlson Comorbidity Index (CCI), which focuses on patients' other medical conditions, and the POSSUM score, which includes both physical health and surgery details. The study aims to see how well these tools predict complications, hospital stay length, and death within 30 days after surgery to help doctors better manage risks. The study observes patients undergoing planned onco-gynecologic surgeries for cancers such as ovarian, cervical, uterine, and vulvar cancer. Researchers will assess each patient using the CCI and POSSUM scores based on their medical history and surgery factors. These scores will then be compared to actual outcomes like surgical complications and mortality. This approach does not involve experimental treatments but uses these risk tools to evaluate their accuracy and usefulness. Participants will be monitored from the day of surgery until hospital discharge, up to 30 days, to track complications, blood loss, blood pressure issues, ICU admissions, reoperations, heart or kidney problems, lung complications, and survival. The study collects detailed clinical data and anesthesia records to compare the two scoring methods. This information aims to improve teamwork among doctors and nurses and enhance patient safety during complex gynecologic cancer surgeries.

CONDITIONS

Brief Title

Comparing CCI and POSSUM for Predicting Oncogynecologic Surgery Complications

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age > 18 years
  • Patient underwent elective onco-gynecologic surgery
Not Eligible

You will not qualify if you...

  • Patient required emergency surgery from any indication
  • Patient chart that not contained primary outcome data eg. absent of the anesthetic record

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) to determine eligibility and review medical history

Surgery and Immediate Post-operative Care

Duration - Up to 30 days from the date of surgery

Participants undergo elective onco-gynecologic surgery with perioperative assessment using CCI and POSSUM scores, followed by monitoring for complications during and immediately after surgery.

1 surgical procedure visit and daily hospital monitoring until discharge, up to 30 days

Post-operative Follow-up

Duration - Up to 30 days post operation

Participants are monitored for surgical complications, recovery progress, and mortality up to 30 days after surgery.

Follow-up visits as part of routine care up to 30 days post surgery

Trial Site Locations

Total: 1 location

1

Faculty of Medicine Siriraj Hospital, Mahidol University

Bangkok, Thailand, 10700

Actively Recruiting

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Research Team

P

Patchareya Nivatpumin, M.D.

J

Jitsupa Nithiuthai, M.D.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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