Actively Recruiting
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
On this page
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
Eligibility Criteria
You may qualify if you...
- Age > 18 years
- Patient underwent elective onco-gynecologic surgery
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
Your Study Journey
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
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
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
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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