Actively Recruiting

Age: 18Years - 85Years
All Genders
NCT07401173

DeepComp for Prediction of Gastric Cancer Postoperative Complications (DeepComp-Prospective)

Led by Qun Zhao · Updated on 2026-04-09

500

Participants Needed

1

Research Sites

8 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Gastric cancer is a leading cause of cancer-related mortality, and radical surgery remains the primary treatment. However, postoperative complications are common and can significantly impact patient recovery and quality of life. Currently, doctors lack precise tools to accurately predict which patients are at high risk for developing severe complications before surgery. This study aims to validate a novel artificial intelligence (AI) model called "DeepComp." The DeepComp model integrates clinical data with advanced radiomic features derived from routine preoperative CT scans. Specifically, it analyzes both the tumor characteristics and the patient's body composition (including skeletal muscle and fat distribution) to assess physiological reserve. In this prospective, multicenter observational study, researchers will enroll patients scheduled for gastric cancer surgery across five medical centers. The DeepComp model will be used to predict the risk of moderate-to-severe postoperative complications (Clavien-Dindo grade II or higher). These predictions will then be compared with the actual clinical outcomes observed 30 days after surgery. The goal is to determine the accuracy and reliability of the DeepComp model in a real-world clinical setting, potentially providing a powerful tool for personalized surgical risk assessment.

CONDITIONS

Official Title

DeepComp for Prediction of Gastric Cancer Postoperative Complications (DeepComp-Prospective)

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Histologically confirmed gastric adenocarcinoma
  • Scheduled for elective radical gastrectomy (open, laparoscopic, or robotic) with curative intent
  • Standard preoperative contrast-enhanced abdominal CT scan (venous phase) within 14 days prior to surgery
  • Willingness to sign informed consent
Not Eligible

You will not qualify if you...

  • Emergency surgery due to perforation, obstruction, or massive bleeding
  • Intraoperative findings of distant metastasis or unresectable disease preventing R0 resection
  • Concurrent or previous malignant tumors within the last 5 years (except gastric cancer)
  • Pregnancy or lactation
  • Severe metallic artifacts on CT images preventing radiomic analysis

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

the Fourth Hospital of Hebei Medical University

Shijiazhuang, None Selected, China, 050011

Actively Recruiting

Loading map...

Research Team

P

Ping'an Ding, PhD

CONTACT

Q

Qun Zhao, PhD

CONTACT

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

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here