Comparative Study on Medical Artificial Intelligence Algorithm Assisted and Conventional Imaging Examination Methods
Comparative Study on the Clinical Efficacy of Medical Artificial Intelligence Algorithm Assisted and Conventional Imaging Examination Methods for Chest Wall Tumor Surgery
1 other identifier
observational
100
0 countries
N/A
Brief Summary
Chest wall tumors are one of the important diseases in thoracic surgery, and surgery remains the main method for treating this disease in clinical practice. The surgery for chest wall tumors requires extensive resection, and more importantly, precise resection. If the resection range is insufficient, it is easy to cause tumor recurrence and metastasis, which affects the patient's survival; If the resection range is too large, it will cause damage to the chest wall structure, affecting the patient's postoperative recovery and quality of life. At present, the determination of the surgical resection range mainly relies on the experience of the surgeon and the results of imaging examinations. Even if experienced surgeons still have multiple imaging examination results, there are still clinical difficulties of insufficient or excessive resection. Medical artificial intelligence is the in-depth application of artificial intelligence technology in the field of medicine. By processing and analyzing massive amounts of medical data, it can accurately locate tumors and optimize surgical plans. Therefore, it is proposed to compare the clinical effects of surgical resection of chest wall tumors using medical artificial intelligence algorithms and conventional imaging examination methods, in order to understand whether it can achieve more accurate tumor resection.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jul 2025
Typical duration for all trials
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 19, 2025
CompletedFirst Posted
Study publicly available on registry
June 27, 2025
CompletedStudy Start
First participant enrolled
July 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2028
ExpectedJune 27, 2025
June 1, 2025
29 days
June 19, 2025
June 19, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Pathological results of surgical margins for chest wall tumors
Pathological diagnosis of residual tissue cells after tumor resection
3 years
Secondary Outcomes (4)
Surgical margins planned by medical artificial intelligence
3 years
Surgical margins planned using conventional imaging techniques
3 years
recurrence-free survival, RFS
3 years
Disease-free survival,DFS
3 years
Study Arms (2)
Medical Artificial Intelligence Algorithm Assistance Group
Before surgery, medical artificial intelligence algorithms are used to outline the resection range of chest wall tumors, while during the actual surgical process, the resection range is determined by intraoperative frozen pathology. Ultimately, the value of medical artificial intelligence algorithm assistance will be evaluated based on paraffin pathology of surgical margins.
Routine imaging examination group
Before surgery, conventional imaging methods are used to outline the resection range of chest wall tumors, while during the actual surgical process, the resection range is determined by intraoperative frozen pathology. The value of routine imaging examination was ultimately evaluated by paraffin pathology of the surgical margin.
Eligibility Criteria
Patients with benign or malignant chest wall tumors require surgical treatment ,meanwhile they have good overall condition and no signs of metastasis,
You may qualify if:
- years old, male or female not limited Anesthesia ASA score I-II Malignant tumor of soft tissue in the chest Malignant tumors of ribs, rib cartilage, and sternum Tumors with uncertain or unknown properties of ribs, rib cartilage, and sternum Giant benign tumors of ribs, rib cartilage, and sternum The preoperative examination results indicate that the tumor has not undergone distant metastasis Willing to participate in the research and sign the informed consent form
You may not qualify if:
- Patients with distant metastasis detected during preoperative examination Inoperable tumor During the examination, it was discovered that the patient had another type of malignant tumor present ECOG 4 Suffering from active or chronic fungal/bacterial/viral infections History of allergy to anesthesia related drugs Heart and lung dysfunction, liver and kidney dysfunction, inability to tolerate surgery Patients with mental disorders who are unable to cooperate with treatment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Target Duration
- 3 Years
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Thoracic Surgery
Study Record Dates
First Submitted
June 19, 2025
First Posted
June 27, 2025
Study Start
July 1, 2025
Primary Completion
July 30, 2025
Study Completion (Estimated)
December 31, 2028
Last Updated
June 27, 2025
Record last verified: 2025-06
Data Sharing
- IPD Sharing
- Will not share