Prediction of Occult Peritoneal Metastasis of Locally Advanced Gastric Cancer Using Multimodal Data Based on Artificial Intelligence Combined With Intraoperative Dynamic Video

NCT ID: NCT06478368

Last Updated: 2025-08-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

1000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-01-01

Study Completion Date

2024-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Brief Summary: Prediction of Occult Peritoneal Metastasis of Locally Advanced Gastric Cancer Using Multimodal Data Based on Artificial Intelligence Combined with Intraoperative Dynamic Video

Gastric cancer, or stomach cancer, is a major health concern worldwide. For patients diagnosed with locally advanced gastric cancer (LAGC), one of the critical challenges is the detection of occult peritoneal metastasis. These metastases are cancerous cells that have spread to the peritoneum (the lining of the abdominal cavity) but are not easily detected by traditional imaging techniques or during surgery. Early and accurate detection of these hidden metastases can greatly influence treatment strategies and improve patient outcomes.

This clinical study explores an innovative approach to address this challenge by combining artificial intelligence (AI) with multimodal data, including intraoperative dynamic video. This method leverages the power of AI to analyze complex and diverse data sources, providing a comprehensive and precise prediction of occult peritoneal metastasis during surgery.

\*\*Hypothesis\*\*

The study hypothesizes that an AI model integrating multimodal data, including intraoperative dynamic video, can accurately predict the presence of occult peritoneal metastasis in patients with locally advanced gastric cancer. By doing so, this approach aims to offer a noninvasive, real-time diagnostic tool that enhances the detection capabilities beyond traditional methods.

Study Design

1. Participants: The study will involve patients diagnosed with locally advanced gastric cancer who are scheduled for surgical treatment. These patients will undergo standard preoperative assessments to confirm their eligibility.
2. Data Collection: During surgery, dynamic video recordings of the abdominal cavity will be captured. Additionally, other relevant multimodal data such as imaging results, histopathological findings, and clinical parameters will be collected.
3. AI Model Development: The collected data will be used to train and validate an AI model. The model will analyze the dynamic video along with other multimodal data to identify patterns and markers indicative of occult peritoneal metastasis.
4. Evaluation and Validation: The AI model's predictions will be compared with the actual surgical and histopathological outcomes to assess its accuracy. The performance of the AI model will be evaluated in terms of sensitivity, specificity, and overall diagnostic accuracy.
5. Outcome Measures: The primary outcome measure will be the accuracy of the AI model in predicting occult peritoneal metastasis. Secondary outcomes will include the impact of this prediction on surgical decision-making, patient outcomes, and potential improvements in survival rates.

Significance

The detection of occult peritoneal metastasis in locally advanced gastric cancer is crucial for effective treatment planning. Traditional diagnostic methods often fail to identify these hidden metastases until they have significantly progressed, limiting treatment options and adversely affecting prognosis. By integrating AI with intraoperative dynamic video and other multimodal data, this study aims to develop a real-time, noninvasive diagnostic tool that can detect these metastases more accurately and earlier than conventional methods.

The potential benefits of this approach include:

* Improved Surgical Decision-Making: Real-time prediction of occult metastasis can inform surgical strategies, enabling more precise and targeted interventions.
* Enhanced Patient Outcomes: Early and accurate detection allows for timely and appropriate treatments, potentially improving survival rates and quality of life for patients.
* Reduced Invasiveness: This method provides a noninvasive means of detecting metastasis, reducing the need for additional invasive procedures.
* Cost-Effectiveness: Early detection and treatment can lower overall healthcare costs by preventing the progression of the disease and reducing the need for extensive treatments at later stages.

Conclusion

This clinical study represents a significant advancement in the field of gastric cancer diagnostics. By leveraging AI to analyze multimodal data, including intraoperative dynamic video, it aims to provide a powerful tool for the early and accurate prediction of occult peritoneal metastasis in patients with locally advanced gastric cancer. The success of this approach could revolutionize the way metastases are detected and managed, ultimately leading to better outcomes for patients.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

This Study Uses AI and Multimodal Data to Noninvasively Detect Occult Peritoneal Metastasis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Laparoscopic exploration

Laparoscopic exploration

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Diagnosis of Locally Advanced Gastric Cancer (LAGC): Patients must have a confirmed diagnosis of locally advanced gastric cancer.
2. Age: Participants must be 18 years or older.
3. Consent: Patients must be able to provide informed consent.
4. Adequate Organ Function: Participants must have sufficient bone marrow, liver, and kidney function, as defined by specific laboratory criteria.
5. Performance Status: Patients should have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2.
6. Willingness to Provide Data: Participants must agree to provide intraoperative dynamic video and other required data for analysis.
7. Scheduled for Surgery: Patients must be scheduled for surgical treatment of their gastric cancer.

Exclusion Criteria

1. Distant Metastases: Patients with confirmed distant metastases (beyond the peritoneum) are excluded.
2. Other Malignancies: Individuals with a history of other malignancies within the past five years, except for adequately treated basal cell or squamous cell skin cancer, or carcinoma in situ of the cervix.
3. Severe Comorbid Conditions: Patients with severe or uncontrolled comorbid conditions, such as significant cardiovascular disease, uncontrolled diabetes, severe infections, or other conditions that could interfere with study participation or outcomes.
4. Pregnancy and Lactation: Pregnant or lactating women are excluded due to potential risks to the fetus or infant.
5. Immunocompromised Status: Patients who are immunocompromised, such as those with HIV/AIDS, or who are receiving immunosuppressive therapy.
6. Concurrent Participation in Other Clinical Trials: Individuals currently participating in another clinical trial that could interfere with this study's procedures or outcomes.
7. Allergies to Study Materials: Patients with known allergies to any components of the study materials used for data collection and analysis.
8. Non-compliance: Individuals deemed unable or unwilling to comply with the study procedures and follow-up requirements.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Qun Zhao

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Qun Zhao

Professor

Responsibility Role SPONSOR_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Department of General Surgery

Shijiazhuang, Hebei, China

Site Status

Countries

Review the countries where the study has at least one active or historical site.

China

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

FUTURE06

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.