Prediction of Postoperative Complications and Survival in Gastric Cancer Using Preoperative Blood Markers
Clinical Study on the Effect of Preoperative Serum Biomarkers on the Prognosis of Gastric Cancer
1 other identifier
observational
3,400
0 countries
N/A
Brief Summary
Gastric cancer is one of the most common cancers worldwide, especially in East Asia. Although surgery remains the main treatment, patients may experience postoperative complications and have varying long-term survival outcomes. Early identification of high-risk patients before surgery is important for improving treatment decisions and patient management. This study aims to develop a prediction model based on routinely available preoperative blood test results and clinical characteristics to estimate the risk of postoperative complications and long-term survival in patients with gastric cancer. The model will be developed and validated using data from multiple medical centers. By using easily accessible clinical information, this study seeks to provide a practical tool to help clinicians better assess patient risk before surgery, support personalized treatment planning, and improve overall patient outcomes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jan 2010
Longer than P75 for all trials
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2024
CompletedFirst Submitted
Initial submission to the registry
November 12, 2024
CompletedFirst Posted
Study publicly available on registry
November 13, 2024
CompletedMarch 3, 2026
February 1, 2026
14.8 years
November 12, 2024
February 27, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
the incidence of gastric cancer
the diagnosis time of gastric cancer
From 18 years old until the developing gastric cancer, through study completion, an average of 5 year.
Interventions
be diagnosed as gastric cancer
Eligibility Criteria
Patients diagnosed with gastric cancer and undergoing radical gastric cancer surgery at the First Hospital of Chongqing Medical University, the Second Hospital of Chongqing Medical University, and the Yongchuan Hospital of Chongqing Medical University.
You may qualify if:
- patients aged ≥18 years;
- patients diagnosed with gastric cancer by pathological biopsy before surgery;
- patients without chemotherapy, radiotherapy, targeted and immunotherapy before enrolment;
- willing to participate in this study and sign the informed consent;
- complete clinical data.
You may not qualify if:
- patients with other primary malignant tumours other than gastric cancer;
- patients with systemic diseases such as severe cardiopulmonary insufficiency that affect the choice of treatment plan;
- patients who are not suitable for enrolment as assessed by the investigator;
- incomplete clinical data.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
November 12, 2024
First Posted
November 13, 2024
Study Start
January 1, 2010
Primary Completion
November 1, 2024
Study Completion
November 1, 2024
Last Updated
March 3, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share
None of the three clinical centres conducting the study allowed the disclosure of patient information and data sharing.